A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6002635



Internal ID21911978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:158081874..158339403hg38UCSC Ensembl
chr6:158502906..158760435hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38257530
hg19257530
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17575273
Samples
Known GenesGTF2H5, SERAC1, SYNJ2, TULP4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6002635
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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