A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16989144



Internal ID60183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:156703838..156703889hg38UCSC Ensembl
chr6:157024972..157025023hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38798
hg19798
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5558338
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16989144
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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