A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv614215



Internal ID16401624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:37058138..37289935hg38UCSC Ensembl
Innerchr9:37058135..37289932hg19UCSC Ensembl
Innerchr9:37048135..37279932hg18UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg38231798
hg19231798
hg18231798
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176450
Samples1780854231_A
Known GenesLOC100506710, ZCCHC7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv614215
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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