A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607669



Internal ID16395078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:79544869..79618804hg38UCSC Ensembl
Innerchr7:79174185..79248120hg19UCSC Ensembl
Innerchr7:79012121..79086056hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3873936
hg1973936
hg1873936
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1155211
Samples1780854341_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607669
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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