A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3674694



Internal ID18972975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:155263540..155284018hg38UCSC Ensembl
Innerchr7:155055250..155075728hg19UCSC Ensembl
Innerchr7:154686183..154706661hg18UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg3820479
hg1920479
hg1820479
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1019278
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3674694
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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