A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527318



Internal ID15454611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:73813198..73837862hg38UCSC Ensembl
Innerchr17:71809337..71834001hg19UCSC Ensembl
Innerchr17:69320932..69345596hg18UCSC Ensembl
Innerchr17:69320932..69345596hg17UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg3824665
hg1924665
hg1824665
hg1724665
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703743
Samples
Known GenesLINC00469
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527318
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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