A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3671054



Internal ID18969335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143755783..143848600hg38UCSC Ensembl
Innerchr7:143452876..143545693hg19UCSC Ensembl
Innerchr7:143083809..143176626hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3892818
hg1992818
hg1892818
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1029574
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)nssv3671054
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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