A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025092



Internal ID18767624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143751274..143877676hg38UCSC Ensembl
Innerchr7:143448367..143574769hg19UCSC Ensembl
Innerchr7:143079300..143205702hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38126403
hg19126403
hg18126403
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6718n100
Supporting Variantsnssv3671046
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)nsv1025092
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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