A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6979729



Internal ID12633963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:42642240..42815941hg38UCSC Ensembl
Innerchr10:43137688..43311389hg19UCSC Ensembl
Innerchr10:42457694..42631395hg18UCSC Ensembl
Innerchr10:42457694..42631395hg17UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38173702
hg19173702
hg18173702
hg17173702
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)essv6979729
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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