A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057725



Internal ID19146944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:27643961..27754003hg38UCSC Ensembl
Innerchr17:25970987..26081029hg19UCSC Ensembl
Innerchr17:22995114..23105156hg18UCSC Ensembl
Cytoband17q11.1
Allele length
AssemblyAllele length
hg38110043
hg19110043
hg18110043
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3136n100
Supporting Variantsnssv3561040
Samples
Known GenesLGALS9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1057725
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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