A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059251



Internal ID19148470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:33332489..33352174hg38UCSC Ensembl
Innerchr17:31659507..31679192hg19UCSC Ensembl
Innerchr17:28683620..28703305hg18UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3819686
hg1919686
hg1819686
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3140n100
Supporting Variantsnssv3561060
Samples
Known GenesASIC2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059251
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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