A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1075608



Internal ID15582108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:163413825..163415602hg38UCSC Ensembl
Innerchr6:163834857..163836634hg19UCSC Ensembl
Innerchr6:163754847..163756624hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg381778
hg191778
hg181778
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv605203
Supporting Variants
Samples
Known GenesCAHM, QKI
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1075608
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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