A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138838



Internal ID338022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:71059432..71059491hg38UCSC Ensembl
chr1:71525115..71525174hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16907263
Samples
Known GenesZRANB2-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138838
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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