A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030567



Internal ID18773098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143733483..143875193hg38UCSC Ensembl
Innerchr7:143430576..143572286hg19UCSC Ensembl
Innerchr7:143061509..143203219hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38141711
hg19141711
hg18141711
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6712n100
Supporting Variantsnssv3754749, nssv3670424
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)nsv1030567
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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