A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007783



Internal ID19097002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:59164119..59199366hg38UCSC Ensembl
Innerchr4:60029837..60065084hg19UCSC Ensembl
Innerchr4:59712432..59747679hg18UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3835248
hg1935248
hg1835248
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3626507
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)nsv1007783
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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