A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17159462



Internal ID21487693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:157420152..157420152hg38UCSC Ensembl
chr6:157841184..157841184hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38106
hg19106
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5628154
Supporting Variants
SamplesNA18534
Known GenesZDHHC14
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17159462
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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