A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002195



Internal ID19091412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:62511213..62547001hg38UCSC Ensembl
Innerchr4:63376931..63412719hg19UCSC Ensembl
Innerchr4:63059526..63095314hg18UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3835789
hg1935789
hg1835789
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5221n100
Supporting Variantsnssv3626521
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)nsv1002195
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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