A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606298



Internal ID16393707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:15558531..15582025hg38UCSC Ensembl
Innerchr7:15598156..15621650hg19UCSC Ensembl
Innerchr7:15564681..15588175hg18UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg3823495
hg1923495
hg1823495
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1079300
Samples
Known GenesAGMO
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606298
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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