A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015673



Internal ID19104891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:8929663..9016071hg38UCSC Ensembl
Innerchr9:8929663..9016071hg19UCSC Ensembl
Innerchr9:8919663..9006071hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3886409
hg1986409
hg1886409
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7396n100
Supporting Variantsnssv3758122
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)nsv1015673
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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