A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6985714



Internal ID12983909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:19469379..19581028hg38UCSC Ensembl
Innerchr7:19509002..19620651hg19UCSC Ensembl
Innerchr7:19475527..19587176hg18UCSC Ensembl
Innerchr7:19282242..19393891hg17UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38111650
hg19111650
hg18111650
hg17111650
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752153
Supporting Variants
SamplesSPC_36
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6985714
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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