A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6985736



Internal ID12637244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:13284601..13405073hg38UCSC Ensembl
Innerchr9:13284600..13405072hg19UCSC Ensembl
Innerchr9:13274600..13395072hg18UCSC Ensembl
Innerchr9:13274600..13395072hg17UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38120473
hg19120473
hg18120473
hg17120473
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752281
Supporting Variants
SamplesSPC_38
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6985736
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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