A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030561



Internal ID19119780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:134721761..134828703hg38UCSC Ensembl
Innerchr4:135642916..135749858hg19UCSC Ensembl
Innerchr4:135862366..135969308hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38106943
hg19106943
hg18106943
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3641104
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)nsv1030561
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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