A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18233651



Internal ID20800691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:26102415..26260224hg38UCSC Ensembl
chr6:26102643..26260452hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg38157810
hg19157810
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6401522
Supporting Variants
Samples
Known GenesHIST1H1D, HIST1H1E, HIST1H1T, HIST1H2AC, HIST1H2AD, HIST1H2AE, HIST1H2BC, HIST1H2BD, HIST1H2BE, HIST1H2BF, HIST1H2BG, HIST1H2BH, HIST1H3D, HIST1H3E, HIST1H3F, HIST1H4C, HIST1H4D, HIST1H4E, HIST1H4F, HIST1H4G
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18233651
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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