A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056524



Internal ID19145743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:73749837..73769576hg38UCSC Ensembl
Innerchr17:71745976..71765715hg19UCSC Ensembl
Innerchr17:69257571..69277310hg18UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg3819740
hg1919740
hg1819740
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3281n100
Supporting Variantsnssv3567783, nssv3567782
Samples
Known GenesLINC00469, LOC100134391
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1056524
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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