A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525983



Internal ID15106590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:241543233..241548401hg38UCSC Ensembl
Innerchr1:241706533..241711701hg19UCSC Ensembl
Innerchr1:239773156..239778324hg18UCSC Ensembl
Innerchr1:238032574..238037742hg17UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg385169
hg195169
hg185169
hg175169
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702202
Samples
Known GenesKMO
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525983
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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