A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999328



Internal ID19158864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:56076751..56175420hg38UCSC Ensembl
Innerchr4:56942917..57041586hg19UCSC Ensembl
Innerchr4:56637674..56736343hg18UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3898670
hg1998670
hg1898670
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5212n100
Supporting Variantsnssv3625282
Samples
Known GenesKIAA1211
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv999328
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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