A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520598



Internal ID15101205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:10469593..10528561hg38UCSC Ensembl
Innerchr6:10469826..10528794hg19UCSC Ensembl
Innerchr6:10577812..10636780hg18UCSC Ensembl
Innerchr6:10577812..10636780hg17UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg3858969
hg1958969
hg1858969
hg1758969
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv373n21
Supporting Variantsnssv693819, nssv702605, nssv704113, nssv672970
Samples
Known GenesGCNT2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520598
Frequency
Sample Size2026
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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