A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3758129



Internal ID18709724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:9793285..9957301hg38UCSC Ensembl
Innerchr9:9793285..9957301hg19UCSC Ensembl
Innerchr9:9783285..9947301hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38164017
hg19164017
hg18164017
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1018814
Supporting Variants
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)nssv3758129
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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