A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6978176



Internal ID12981541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:57142434..57177134hg38UCSC Ensembl
Innerchr10:58902194..58936894hg19UCSC Ensembl
Innerchr10:58572200..58606900hg18UCSC Ensembl
Innerchr10:58572200..58606900hg17UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3834701
hg1934701
hg1834701
hg1734701
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34869
Supporting Variants
SamplesNA18974
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6978176
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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