A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3569697



Internal ID18867978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42816973..43236801hg38UCSC Ensembl
Innerchr19:43321125..43740953hg19UCSC Ensembl
Innerchr19:48012965..48432793hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38419829
hg19419829
hg18419829
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1062897
Supporting Variants
Samples
Known GenesLOC100289650, LOC284344, PSG1, PSG10P, PSG11, PSG2, PSG4, PSG5, 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)nssv3569697
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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