A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602109



Internal ID16042832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32190542..32193653hg38UCSC Ensembl
Innerchr6:32158319..32161430hg19UCSC Ensembl
Innerchr6:32266297..32269408hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg383112
hg193112
hg183112
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1053910, nssv1053911
Samples
Known GenesGPSM3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602109
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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