A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv529004



Internal ID15109611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:30992197..31700936hg38UCSC Ensembl
Innerchr11:31013744..31722484hg19UCSC Ensembl
Innerchr11:30970320..31679060hg18UCSC Ensembl
Innerchr11:30970320..31679060hg17UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38708740
hg19708741
hg18708741
hg17708741
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705711
Samples
Known GenesDCDC1, DCDC5, DNAJC24, ELP4, IMMP1L
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv529004
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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