A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024496



Internal ID18767028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143733941..143870954hg38UCSC Ensembl
Innerchr7:143431034..143568047hg19UCSC Ensembl
Innerchr7:143061967..143198980hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38137014
hg19137014
hg18137014
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6712n100
Supporting Variantsnssv3670425
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)nsv1024496
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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