A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608981



Internal ID16396390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:149749157..149816064hg38UCSC Ensembl
Innerchr7:149446246..149513152hg19UCSC Ensembl
Innerchr7:149077179..149144085hg18UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3866908
hg1966907
hg1866907
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11715n54
Supporting Variantsnssv1155692
SamplesHGDP00830
Known GenesSSPO, ZNF467
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608981
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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