A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056270



Internal ID18798801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42634891..43038667hg38UCSC Ensembl
Innerchr19:43139043..43542819hg19UCSC Ensembl
Innerchr19:47830883..48234659hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38403777
hg19403777
hg18403777
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3722784
Samples
Known GenesLIPE-AS1, LOC100289650, PSG1, PSG10P, PSG11, PSG3, PSG6, PSG7, PSG8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1056270
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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