A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6985445



Internal ID12982328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:30255402..30384202hg38UCSC Ensembl
Innerchr9:30255400..30384200hg19UCSC Ensembl
Innerchr9:30245400..30374200hg18UCSC Ensembl
Innerchr9:30245400..30374200hg17UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38128801
hg19128801
hg18128801
hg17128801
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv35141
Supporting Variants
SamplesNA19152
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6985445
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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