A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607705



Internal ID16395114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:83240806..83279561hg38UCSC Ensembl
Innerchr7:82870122..82908877hg19UCSC Ensembl
Innerchr7:82708058..82746813hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3838756
hg1938756
hg1838756
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1155226
Samples1780862088_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607705
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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