A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6982365



Internal ID12626941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:44699737..44846912hg38UCSC Ensembl
Innerchr10:45195185..45342360hg19UCSC Ensembl
Innerchr10:44515191..44662366hg18UCSC Ensembl
Innerchr10:44515191..44662366hg17UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38147176
hg19147176
hg18147176
hg17147176
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2750893
Supporting Variants
SamplesBEC_428
Known GenesTMEM72-AS1
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6982365
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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