A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022686



Internal ID19111904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143747111..143875193hg38UCSC Ensembl
Innerchr7:143444204..143572286hg19UCSC Ensembl
Innerchr7:143075137..143203219hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38128083
hg19128083
hg18128083
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6717n100
Supporting Variantsnssv3670977, nssv3670982, nssv3670978, nssv3670981, nssv3670980, nssv3754798, nssv3670979
Samples
Known GenesCTAGE6, FAM115A, LOC154761
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1022686
Frequency
Sample Size11257
Observed Gain3
Observed Loss4
Observed Complex0
Frequencyn/a


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