A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv662951



Internal ID15399603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:106236120..106255743hg38UCSC Ensembl
Innerchr6:106683995..106703618hg19UCSC Ensembl
Innerchr6:106790688..106810311hg18UCSC Ensembl
Innerchr6:106790688..106810311hg17UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3819624
hg1919624
hg1819624
hg1719624
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520329
Supporting Variants
Samples
Known GenesATG5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv662951
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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