A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1817496



Internal ID17826621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:220253472..220261337hg38UCSC Ensembl
Innerchr1:220426814..220434679hg19UCSC Ensembl
Innerchr1:218493437..218501302hg18UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg387866
hg197866
hg187866
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv945297
Supporting Variants
SamplesHGDP00998
Known GenesRAB3GAP2
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Commentslineage specific duplication - fixed_Pab-Ppy-Ggod-Ggog-Gbeg-Ptrs-Ptrt-Ptre-Ptrv-Ppa-Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv1817496
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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