A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025772



Internal ID19114989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:9799050..9822041hg38UCSC Ensembl
Innerchr9:9799050..9822041hg19UCSC Ensembl
Innerchr9:9789050..9812041hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3822992
hg1922992
hg1822992
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7398n100
Supporting Variantsnssv3689167, nssv3689166
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)nsv1025772
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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