A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614604



Internal ID16402013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:71142654..71153632hg38UCSC Ensembl
Innerchr9:73757570..73768548hg19UCSC Ensembl
Innerchr9:72947390..72958368hg18UCSC Ensembl
Cytoband9q21.12
Allele length
AssemblyAllele length
hg3810979
hg1910979
hg1810979
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12749n54
Supporting Variantsnssv1176089
SamplesNINDS_174
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614604
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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