A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3754682



Internal ID18706277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143521753..143701114hg38UCSC Ensembl
Innerchr7:143218846..143398207hg19UCSC Ensembl
Innerchr7:142928968..143029140hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38179362
hg19179362
hg18100173
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1017872
Supporting Variants
Samples
Known GenesCTAGE15, EPHA1-AS1, FAM115C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3754682
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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