A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032107



Internal ID19121329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:11975273..12379463hg38UCSC Ensembl
Innerchr9:11975273..12379463hg19UCSC Ensembl
Innerchr9:11965273..12369463hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38404191
hg19404191
hg18404191
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7426n100
Supporting Variantsnssv3758200, nssv3690519, nssv3690520
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1032107
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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