A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613949



Internal ID16401358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:27250870..27353462hg38UCSC Ensembl
Innerchr9:27250868..27353460hg19UCSC Ensembl
Innerchr9:27240868..27343460hg18UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg38102593
hg19102593
hg18102593
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156751
Samples1780862529_A
Known GenesEQTN, LINC00032, MOB3B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613949
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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