A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3671017



Internal ID18969298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143751274..143833864hg38UCSC Ensembl
Innerchr7:143448367..143530957hg19UCSC Ensembl
Innerchr7:143079300..143161890hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3882591
hg1982591
hg1882591
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1018338
Supporting Variants
Samples
Known GenesCTAGE6, LOC154761
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3671017
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