A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699785



Internal ID15089751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:90357904..91080775hg38UCSC Ensembl
Innerchr6:91067623..91790493hg19UCSC Ensembl
Innerchr6:91124344..91847214hg18UCSC Ensembl
Innerchr6:91124344..91847214hg17UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38722872
hg19722871
hg18722871
hg17722871
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523939
Supporting Variants
Samples
Known GenesMAP3K7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699785
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer