A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011482



Internal ID19100699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:435303..481679hg38UCSC Ensembl
Innerchr4:429092..475468hg19UCSC Ensembl
Innerchr4:419092..465468hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3846377
hg1946377
hg1846377
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5078n100
Supporting Variantsnssv3738103
Samples
Known GenesABCA11P, ZNF721
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1011482
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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