A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527127



Internal ID15107734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:127271203..127297045hg38UCSC Ensembl
Innerchr9:130033482..130059324hg19UCSC Ensembl
Innerchr9:129073303..129099145hg18UCSC Ensembl
Innerchr9:127113036..127138878hg17UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3825843
hg1925843
hg1825843
hg1725843
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703512
Samples
Known GenesGARNL3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527127
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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