A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524392



Internal ID15104999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:114865252..114917448hg38UCSC Ensembl
Innerchr1:115407873..115460069hg19UCSC Ensembl
Innerchr1:115209396..115261592hg18UCSC Ensembl
Innerchr1:115119915..115172111hg17UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg3852197
hg1952197
hg1852197
hg1752197
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700309
Samples
Known GenesSYCP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524392
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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