A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607716



Internal ID16395125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:85449307..85470582hg38UCSC Ensembl
Innerchr7:85078623..85099898hg19UCSC Ensembl
Innerchr7:84916559..84937834hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3821276
hg1921276
hg1821276
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1089376
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607716
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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