A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516902



Internal ID15444195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:106656499..106667519hg38UCSC Ensembl
Innerchr6:107104374..107115394hg19UCSC Ensembl
Innerchr6:107211067..107222087hg18UCSC Ensembl
Innerchr6:107211067..107222087hg17UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3811021
hg1911021
hg1811021
hg1711021
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv654786, nssv676647, nssv678541, nssv692586, nssv682470
Samples
Known GenesQRSL1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516902
Frequency
Sample Size2026
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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