A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6076661



Internal ID21985894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:157420485..157420485hg38UCSC Ensembl
chr6:157841517..157841517hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17562379
Samples
Known GenesZDHHC14
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6076661
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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