A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv665299



Internal ID15055265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:57434294..61063311hg38UCSC Ensembl
Innerchr6:57299092..58031058hg19UCSC Ensembl
Innerchr6:57407051..58139017hg18UCSC Ensembl
Innerchr6:57407051..58139017hg17UCSC Ensembl
Cytoband6p11.2
Allele length
AssemblyAllele length
hg383629018
hg19731967
hg18731967
hg17731967
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515916
Supporting Variants
Samples
Known GenesPRIM2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv665299
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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