A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055587



Internal ID19144806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42864771..42963703hg38UCSC Ensembl
Innerchr19:43368923..43467855hg19UCSC Ensembl
Innerchr19:48060763..48159695hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3898933
hg1998933
hg1898933
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3570129
Samples
Known GenesPSG1, 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)nsv1055587
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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