A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017807



Internal ID19107024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143534121..143816712hg38UCSC Ensembl
Innerchr7:143231214..143513805hg19UCSC Ensembl
Innerchr7:142941336..143144738hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38282592
hg19282592
hg18203403
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6702n100
Supporting Variantsnssv3670357, nssv3670358
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)nsv1017807
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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