A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024467



Internal ID18766999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143751274..143875193hg38UCSC Ensembl
Innerchr7:143448367..143572286hg19UCSC Ensembl
Innerchr7:143079300..143203219hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38123920
hg19123920
hg18123920
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6712n100
Supporting Variantsnssv3671045
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)nsv1024467
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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