A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030657



Internal ID19119876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:10002355..10481262hg38UCSC Ensembl
Innerchr9:10002355..10481262hg19UCSC Ensembl
Innerchr9:9992355..10471262hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38478908
hg19478908
hg18478908
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3758150
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)nsv1030657
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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