A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606712



Internal ID16394121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:40332994..40387401hg38UCSC Ensembl
Innerchr7:40372593..40427000hg19UCSC Ensembl
Innerchr7:40339118..40393525hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3854408
hg1954408
hg1854408
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11291n54
Supporting Variantsnssv1083048
Samples
Known GenesC7orf10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606712
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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