A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6979730



Internal ID12633962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:42730246..42815946hg38UCSC Ensembl
Innerchr10:43225694..43311394hg19UCSC Ensembl
Innerchr10:42545700..42631400hg18UCSC Ensembl
Innerchr10:42545700..42631400hg17UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3885701
hg1985701
hg1885701
hg1785701
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34929
Supporting Variants
SamplesNA18620
Known GenesBMS1
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6979730
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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