A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17037055



Internal ID92458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:74744656..74745536hg38UCSC Ensembl
chr10:76504414..76505294hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38881
hg19881
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5559216
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17037055
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.004839


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