A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3722927



Internal ID19021208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42790226..43038667hg38UCSC Ensembl
Innerchr19:43294378..43542819hg19UCSC Ensembl
Innerchr19:47986218..48234659hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38248442
hg19248442
hg18248442
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1061984
Supporting Variants
Samples
Known GenesLOC100289650, PSG1, PSG10P, PSG11, 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)nssv3722927
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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