A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3722971



Internal ID19021252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42790226..43285762hg38UCSC Ensembl
Innerchr19:43294378..43789914hg19UCSC Ensembl
Innerchr19:47986218..48481754hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38495537
hg19495537
hg18495537
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1066512
Supporting Variants
Samples
Known GenesLOC100289650, LOC284344, PSG1, PSG10P, PSG11, PSG2, PSG4, PSG5, PSG6, PSG7, PSG9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3722971
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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