A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv652271



Internal ID15388923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:108873603..108923441hg38UCSC Ensembl
Innerchr1:109416225..109466063hg19UCSC Ensembl
Innerchr1:109217748..109267586hg18UCSC Ensembl
Innerchr1:109128267..109178105hg17UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3849839
hg1949839
hg1849839
hg1749839
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517523
Supporting Variants
Samples
Known GenesGPSM2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv652271
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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