A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528054



Internal ID15455347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:88717509..88722643hg38UCSC Ensembl
Innerchr6:89427228..89432362hg19UCSC Ensembl
Innerchr6:89483947..89489081hg18UCSC Ensembl
Innerchr6:89483947..89489081hg17UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg385135
hg195135
hg185135
hg175135
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704587
Samples
Known GenesRNGTT
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528054
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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