A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613657



Internal ID16401066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:15615323..15727520hg38UCSC Ensembl
Innerchr9:15615321..15727518hg19UCSC Ensembl
Innerchr9:15605321..15717518hg18UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg38112198
hg19112198
hg18112198
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12575n54
Supporting Variantsnssv1128807, nssv1156734
SamplesNINDS_42
Known GenesCCDC171
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613657
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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