A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527897



Internal ID15108504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:1606964..1638896hg38UCSC Ensembl
Innerchr17:1510258..1542190hg19UCSC Ensembl
Innerchr17:1457008..1488940hg18UCSC Ensembl
Innerchr17:1457008..1488940hg17UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3831933
hg1931933
hg1831933
hg1731933
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704401
Samples
Known GenesSCARF1, SLC43A2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527897
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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