A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528699



Internal ID15455992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:11989417..12029858hg38UCSC Ensembl
Innerchr18:11989416..12029857hg19UCSC Ensembl
Innerchr18:11979416..12019857hg18UCSC Ensembl
Innerchr18:11979416..12019857hg17UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3840442
hg1940442
hg1840442
hg1740442
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705345
Samples
Known GenesIMPA2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528699
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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