A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6983548



Internal ID12976471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:7260390..7390841hg38UCSC Ensembl
Innerchr9:7260390..7390841hg19UCSC Ensembl
Innerchr9:7250390..7380841hg18UCSC Ensembl
Innerchr9:7250390..7380841hg17UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38130452
hg19130452
hg18130452
hg17130452
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752310
Supporting Variants
SamplesBEC_667
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6983548
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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