A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3670332



Internal ID18621927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143530012..143826103hg38UCSC Ensembl
Innerchr7:143227105..143523196hg19UCSC Ensembl
Innerchr7:142937227..143154129hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38296092
hg19296092
hg18216903
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1021830
Supporting Variants
Samples
Known GenesCTAGE15, CTAGE6, FAM115C, LOC154761
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3670332
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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