A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999771



Internal ID19159307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:120600739..120626294hg38UCSC Ensembl
Innerchr4:121521894..121547449hg19UCSC Ensembl
Innerchr4:121741344..121766899hg18UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg3825556
hg1925556
hg1825556
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5375n100
Supporting Variantsnssv3639354
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)nsv999771
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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