A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608340



Internal ID16395749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:124498133..124556390hg38UCSC Ensembl
Innerchr7:124138187..124196444hg19UCSC Ensembl
Innerchr7:123925423..123983680hg18UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg3858258
hg1958258
hg1858258
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1093601
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608340
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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