A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024538



Internal ID19113755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:64683555..64903011hg38UCSC Ensembl
Innerchr9:69695973..69915429hg19UCSC Ensembl
Innerchr9:68985793..69205249hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38219457
hg19219457
hg18219457
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7660n100
Supporting Variantsnssv3696159, nssv3696160
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)nsv1024538
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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