A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608335



Internal ID16395744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:122109909..122139431hg38UCSC Ensembl
Innerchr7:121749963..121779485hg19UCSC Ensembl
Innerchr7:121537199..121566721hg18UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg3829523
hg1929523
hg1829523
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1093596
Samples
Known GenesAASS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608335
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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