A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034865



Internal ID18777397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143582086..143835893hg38UCSC Ensembl
Innerchr7:143279179..143532986hg19UCSC Ensembl
Innerchr7:142989301..143163919hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38253808
hg19253808
hg18174619
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3670410
Samples
Known GenesCTAGE6, 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)nsv1034865
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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