A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977133



Internal ID18612339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:15821858..15837478hg38UCSC Ensembl
Innerchr12:15974792..15990412hg19UCSC Ensembl
Innerchr12:15866059..15881679hg18UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg3815621
hg1915621
hg1815621
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2758364
SamplesHGDP00998
Known Genes
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv977133
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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