A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013884



Internal ID19103103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:61673241..61732899hg38UCSC Ensembl
Innerchr3:61658915..61718573hg19UCSC Ensembl
Innerchr3:61633955..61693613hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3859659
hg1959659
hg1859659
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3593436
Samples
Known GenesPTPRG
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1013884
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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