A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029900



Internal ID19119119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:46587..208456hg38UCSC Ensembl
Innerchr9:46587..208456hg19UCSC Ensembl
Innerchr9:36587..198456hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38161870
hg19161870
hg18161870
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7343n100
Supporting Variantsnssv3690931, nssv3690933, nssv3690930, nssv3690932, nssv3690934
Samples
Known GenesCBWD1, FOXD4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1029900
Frequency
Sample Size11257
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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