A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2703942



Internal ID17784271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:181467855..181478259hg38UCSC Ensembl
Innerchr5:180894856..180905260hg19UCSC Ensembl
Innerchr5:180827462..180837969hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3810405
hg1910405
hg1810508
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv965051
Supporting Variants
SamplesHGDP00665
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Commentslineage specific expansions - expansion_Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2703942
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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