A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607396



Internal ID16394805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:66122550..66126323hg38UCSC Ensembl
Innerchr7:65587537..65591310hg19UCSC Ensembl
Innerchr7:65224972..65228745hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg383774
hg193774
hg183774
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1085613
Samples
Known GenesCRCP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607396
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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