A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv679099



Internal ID15069065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:92554588..94746156hg38UCSC Ensembl
Innerchr6:93264306..95455874hg19UCSC Ensembl
Innerchr6:93321027..95512595hg18UCSC Ensembl
Innerchr6:93321027..95512595hg17UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg382191569
hg192191569
hg182191569
hg172191569
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517329
Supporting Variants
Samples
Known GenesEPHA7, TSG1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv679099
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