A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520425



Internal ID15101032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:150697476..150701208hg38UCSC Ensembl
Innerchr1:150669952..150673684hg19UCSC Ensembl
Innerchr1:148936576..148940308hg18UCSC Ensembl
Innerchr1:147483025..147486757hg17UCSC Ensembl
Cytoband1q21.2
Allele length
AssemblyAllele length
hg383733
hg193733
hg183733
hg173733
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv678859, nssv671343
Samples
Known GenesHORMAD1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520425
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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