A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055870



Internal ID19145089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:44392222..44434604hg38UCSC Ensembl
Innerchr19:44896386..44938779hg19UCSC Ensembl
Innerchr19:49588226..49630619hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3842383
hg1942394
hg1842394
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3605n100
Supporting Variantsnssv3573787, nssv3573790, nssv3573788, nssv3573789
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)nsv1055870
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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