A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4737645



Internal ID20513607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:157522738..157522837hg38UCSC Ensembl
chr6:157943770..157943869hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16276959
Samples
Known GenesZDHHC14
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4737645
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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