A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6979632



Internal ID12633837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:19520765..19686665hg38UCSC Ensembl
Innerchr10:19809694..19975594hg19UCSC Ensembl
Innerchr10:19849700..20015600hg18UCSC Ensembl
Innerchr10:19849700..20015600hg17UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38165901
hg19165901
hg18165901
hg17165901
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34306
Supporting Variants
SamplesNA18592
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6979632
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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