A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6979039



Internal ID12632837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:38599303..38682003hg38UCSC Ensembl
Innerchr9:38599300..38682000hg19UCSC Ensembl
Innerchr9:38589300..38672000hg18UCSC Ensembl
Innerchr9:38589300..38672000hg17UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg3882701
hg1982701
hg1882701
hg1782701
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv35073
Supporting Variants
SamplesNA12864
Known GenesANKRD18A, FAM201A
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6979039
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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