A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034767



Internal ID18777300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143733941..143877676hg38UCSC Ensembl
Innerchr7:143431034..143574769hg19UCSC Ensembl
Innerchr7:143061967..143205702hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38143736
hg19143736
hg18143736
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6712n100
Supporting Variantsnssv3670426
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)nsv1034767
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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