A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034821



Internal ID19124042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:9798243..9822041hg38UCSC Ensembl
Innerchr9:9798243..9822041hg19UCSC Ensembl
Innerchr9:9788243..9812041hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3823799
hg1923799
hg1823799
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7398n100
Supporting Variantsnssv3689145, nssv3689152, nssv3689157, nssv3689147, nssv3689151, nssv3689149, nssv3689162, nssv3689165, nssv3689163, nssv3689159, nssv3758131, nssv3689155, nssv3689154, nssv3758132, nssv3758135, nssv3689146, nssv3689153, nssv3689161, nssv3689156, nssv3689160, nssv3689144, nssv3689150, nssv3689164, nssv3689158, nssv3758133, nssv3758134, nssv3689148
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)nsv1034821
Frequency
Sample Size11257
Observed Gain0
Observed Loss27
Observed Complex0
Frequencyn/a


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