A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029341



Internal ID19118560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:11459329..11631105hg38UCSC Ensembl
Innerchr9:11459329..11631105hg19UCSC Ensembl
Innerchr9:11449329..11621105hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38171777
hg19171777
hg18171777
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7411n100
Supporting Variantsnssv3689235, nssv3689236
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)nsv1029341
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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