A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066685



Internal ID19155904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42882021..43029263hg38UCSC Ensembl
Innerchr19:43386173..43533415hg19UCSC Ensembl
Innerchr19:48078013..48225255hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38147243
hg19147243
hg18147243
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3575n100
Supporting Variantsnssv3570148
Samples
Known GenesPSG11, PSG6, PSG7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066685
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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