A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2033830



Internal ID17881552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:82810618..82827409hg38UCSC Ensembl
Innerchr15:83479370..83496161hg19UCSC Ensembl
Innerchr15:81276424..81293215hg18UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg3816792
hg1916792
hg1816792
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv977747
Supporting Variants
SamplesHGDP01307
Known GenesWHAMM
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)nssv2033830
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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