A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6979740



Internal ID12633988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31391844..31483744hg38UCSC Ensembl
Innerchr6:31359621..31451521hg19UCSC Ensembl
Innerchr6:31467600..31559500hg18UCSC Ensembl
Innerchr6:31467600..31559500hg17UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3891901
hg1991901
hg1891901
hg1791901
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34991
Supporting Variants
SamplesNA18620
Known GenesHCG26, HCP5, MICA
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6979740
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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