A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608975



Internal ID16049698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:149192999..149250188hg38UCSC Ensembl
Innerchr7:148890091..148947279hg19UCSC Ensembl
Innerchr7:148521024..148578212hg18UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3857190
hg1957189
hg1857189
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11712n54
Supporting Variantsnssv1155691
Samples1780862101_A
Known GenesZNF212, ZNF282
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608975
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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