A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3612634



Internal ID6652847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:26301213..26309862hg38UCSC Ensembl
chr7:26340833..26349482hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg388650
hg198650
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12710583
SamplesHG01948
Known GenesSNX10
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3612634
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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