A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019550



Internal ID19108768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143549301..143833864hg38UCSC Ensembl
Innerchr7:143246394..143530957hg19UCSC Ensembl
Innerchr7:142956516..143161890hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38284564
hg19284564
hg18205375
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6702n100
Supporting Variantsnssv3670396, nssv3670395
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)nsv1019550
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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