A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607724



Internal ID16395133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:86124459..86322767hg38UCSC Ensembl
Innerchr7:85753775..85952083hg19UCSC Ensembl
Innerchr7:85591711..85790019hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38198309
hg19198309
hg18198309
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1089385
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607724
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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