A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3608726



Internal ID6995650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:37993776..38019902hg38UCSC Ensembl
chr6:37961552..37987678hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg3826127
hg1926127
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12322498, essv12322488, essv12322499, essv12322487, essv12322501, essv12322504, essv12322505, essv12322503, essv12322493, essv12322515, essv12322512, essv12322486, essv12322514, essv12322497, essv12322485, essv12322489, essv12322510, essv12322513, essv12322509, essv12322507, essv12322500, essv12322506, essv12322491, essv12322484, essv12322511, essv12322492, essv12322502, essv12322496, essv12322508, essv12322494, essv12322495, essv12322490
SamplesHG00542, NA18603, NA19057, HG01140, HG00663, NA19792, NA19746, NA19764, HG01997, HG02146, HG02521, HG02130, HG02301, NA18571, NA19681, HG01892, HG02260, HG01942, HG00543, HG01435, HG02513, HG02090, HG01029, NA18626, HG02121, HG01921, NA19761, HG01951, HG02274, NA19780, HG01566, HG02406
Known GenesZFAND3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3608726
Frequency
Sample Size2504
Observed Gain32
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer