A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3571606



Internal ID18869887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42790226..43004881hg38UCSC Ensembl
Innerchr19:43294378..43509033hg19UCSC Ensembl
Innerchr19:47986218..48200873hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38214656
hg19214656
hg18214656
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1059684
Supporting Variants
Samples
Known GenesLOC100289650, PSG1, PSG10P, 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)nssv3571606
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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