A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023836



Internal ID19113053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:646024..877740hg38UCSC Ensembl
Innerchr9:646024..877740hg19UCSC Ensembl
Innerchr9:636024..867740hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38231717
hg19231717
hg18231717
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3758074
Samples
Known GenesDMRT1, KANK1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1023836
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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