A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024501



Internal ID19113718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143534121..143833864hg38UCSC Ensembl
Innerchr7:143231214..143530957hg19UCSC Ensembl
Innerchr7:142941336..143161890hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38299744
hg19299744
hg18220555
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6702n100
Supporting Variantsnssv3754747, nssv3670360
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)nsv1024501
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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