A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3571227



Internal ID18869508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42790226..43029962hg38UCSC Ensembl
Innerchr19:43294378..43534114hg19UCSC Ensembl
Innerchr19:47986218..48225954hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38239737
hg19239737
hg18239737
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1058522
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)nssv3571227
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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