A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2406397



Internal ID17770766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:35469687..35470884hg38UCSC Ensembl
Innerchr6:35437464..35438661hg19UCSC Ensembl
Innerchr6:35545442..35546639hg18UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg381198
hg191198
hg181198
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv965717
Supporting Variants
SamplesHGDP00542
Known GenesMIR7111, RPL10A
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)nssv2406397
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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