A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9872829



Internal ID6498122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:16936619..16947018hg38UCSC Ensembl
chr1:17263114..17273513hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3810400
hg1910400
Variant TypeCNV gain
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3585355
Supporting Variants
SamplesHG00463
Known GenesCROCC
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv9872829
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