A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607717



Internal ID16395126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:85535973..85620839hg38UCSC Ensembl
Innerchr7:85165289..85250155hg19UCSC Ensembl
Innerchr7:85003225..85088091hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3884867
hg1984867
hg1884867
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1089377
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607717
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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