A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6986011



Internal ID12635881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:112621052..112811009hg38UCSC Ensembl
Innerchr9:115383332..115573289hg19UCSC Ensembl
Innerchr9:114423153..114613110hg18UCSC Ensembl
Innerchr9:112462887..112652844hg17UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38189958
hg19189958
hg18189958
hg17189958
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv35051
Supporting Variants
SamplesNA19204
Known GenesINIP, KIAA1958, SNX30
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6986011
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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