A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527805



Internal ID15455098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:241487718..241493385hg38UCSC Ensembl
Innerchr1:241651018..241656685hg19UCSC Ensembl
Innerchr1:239717641..239723308hg18UCSC Ensembl
Innerchr1:237977059..237982726hg17UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg385668
hg195668
hg185668
hg175668
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704299
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527805
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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