A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062330



Internal ID18804861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:44359787..44434102hg38UCSC Ensembl
Innerchr19:44863939..44938277hg19UCSC Ensembl
Innerchr19:49555779..49630117hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3874316
hg1974339
hg1874339
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3724891
Samples
Known GenesZNF229, ZNF285
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1062330
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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