A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024360



Internal ID18766893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143549301..143780696hg38UCSC Ensembl
Innerchr7:143246394..143477789hg19UCSC Ensembl
Innerchr7:142956516..143108722hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38231396
hg19231396
hg18152207
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3670384, nssv3670383, nssv3670382
Samples
Known GenesCTAGE15, CTAGE6, FAM115C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1024360
Frequency
Sample Size29084
Observed Gain2
Observed Loss1
Observed Complex0
Frequencyn/a


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