A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516177



Internal ID15096784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:110752160..110789924hg38UCSC Ensembl
Innerchr6:111073363..111111127hg19UCSC Ensembl
Innerchr6:111180056..111217820hg18UCSC Ensembl
Innerchr6:111180056..111217820hg17UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3837765
hg1937765
hg1837765
hg1737765
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv666636, nssv693807
Samples
Known GenesCDK19
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516177
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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