A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015674



Internal ID18758208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143525976..143875193hg38UCSC Ensembl
Innerchr7:143223069..143572286hg19UCSC Ensembl
Innerchr7:142933191..143203219hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38349218
hg19349218
hg18270029
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6700n100
Supporting Variantsnssv3670307, nssv3670306
Samples
Known GenesCTAGE15, CTAGE6, FAM115A, 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)nsv1015674
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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