A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024714



Internal ID19113931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143525976..143870954hg38UCSC Ensembl
Innerchr7:143223069..143568047hg19UCSC Ensembl
Innerchr7:142933191..143198980hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38344979
hg19344979
hg18265790
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6700n100
Supporting Variantsnssv3754736, nssv3670302, nssv3754738, nssv3670301, nssv3670304, nssv3670300, nssv3670305, nssv3754737, nssv3670303
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)nsv1024714
Frequency
Sample Size11257
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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