A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605196



Internal ID16392605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:163413723..163414407hg38UCSC Ensembl
Innerchr6:163834755..163835439hg19UCSC Ensembl
Innerchr6:163754745..163755429hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38685
hg19685
hg18685
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1075598, nssv1075599, nssv1075597
Samples
Known GenesCAHM
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605196
Frequency
Sample Size17421
Observed Gain1
Observed Loss2
Observed Complex0
Frequencyn/a


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