A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615991



Internal ID16056714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:136972675..137011907hg38UCSC Ensembl
Innerchr9:139867127..139906359hg19UCSC Ensembl
Innerchr9:138986948..139026180hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3839233
hg1939233
hg1839233
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1148343
Samples
Known GenesABCA2, C9orf142, CLIC3, LCNL1, PTGDS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615991
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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