A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032019



Internal ID19121241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:9919783..10070211hg38UCSC Ensembl
Innerchr9:9919783..10070211hg19UCSC Ensembl
Innerchr9:9909783..10060211hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38150429
hg19150429
hg18150429
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7400n100
Supporting Variantsnssv3758144
Samples
Known GenesPTPRD
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1032019
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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