A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3570194



Internal ID18868475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42978334..43134772hg38UCSC Ensembl
Innerchr19:43482486..43638924hg19UCSC Ensembl
Innerchr19:48174326..48330764hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38156439
hg19156439
hg18156439
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1060797
Supporting Variants
Samples
Known GenesPSG11, PSG2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3570194
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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