A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605197



Internal ID16045920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:163413723..163414813hg38UCSC Ensembl
Innerchr6:163834755..163835845hg19UCSC Ensembl
Innerchr6:163754745..163755835hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg381091
hg191091
hg181091
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11025n54
Supporting Variantsnssv1075600
Samples
Known GenesCAHM, QKI
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605197
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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