A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022365



Internal ID19111583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143525976..143827101hg38UCSC Ensembl
Innerchr7:143223069..143524194hg19UCSC Ensembl
Innerchr7:142933191..143155127hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38301126
hg19301126
hg18221937
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6702n100
Supporting Variantsnssv3670256, nssv3670255, nssv3670248, nssv3670251, nssv3670252, nssv3670249, nssv3670246, nssv3670247, nssv3754726, nssv3670250, nssv3754725, nssv3670254, nssv3670253
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)nsv1022365
Frequency
Sample Size11257
Observed Gain13
Observed Loss0
Observed Complex0
Frequencyn/a


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