A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16952103



Internal ID35426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:71007356..71007407hg38UCSC Ensembl
chr4:71873073..71873124hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg38676
hg19676
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5559743
Supporting Variants
Samples
Known GenesDCK
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16952103
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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