A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021214



Internal ID19110432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:8929663..9011443hg38UCSC Ensembl
Innerchr9:8929663..9011443hg19UCSC Ensembl
Innerchr9:8919663..9001443hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3881781
hg1981781
hg1881781
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7396n100
Supporting Variantsnssv3689123
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)nsv1021214
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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