A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008614



Internal ID19097831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:29211575..29246383hg38UCSC Ensembl
Innerchr4:29213197..29248005hg19UCSC Ensembl
Innerchr4:28822295..28857103hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3834809
hg1934809
hg1834809
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3620629
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1008614
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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