A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023460



Internal ID19112677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:924525..953746hg38UCSC Ensembl
Innerchr9:924525..953746hg19UCSC Ensembl
Innerchr9:914525..943746hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg3829222
hg1929222
hg1829222
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3691209, nssv3758075, nssv3691207, nssv3691208
Samples
Known GenesDMRT1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1023460
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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