A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1000785



Internal ID19090002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:126218188..126362145hg38UCSC Ensembl
Innerchr4:127139343..127283300hg19UCSC Ensembl
Innerchr4:127358793..127502750hg18UCSC Ensembl
Cytoband4q28.1
Allele length
AssemblyAllele length
hg38143958
hg19143958
hg18143958
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3639422
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)nsv1000785
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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