A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576069



Internal ID16016792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:76856392..76889866hg38UCSC Ensembl
Innerchr17:74852474..74885948hg19UCSC Ensembl
Innerchr17:72364069..72397543hg18UCSC Ensembl
Cytoband17q25.2
Allele length
AssemblyAllele length
hg3833475
hg1933475
hg1833475
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv876220
Samples
Known GenesMGAT5B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576069
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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