A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16897705



Internal ID172630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:244750940..244751142hg38UCSC Ensembl
chr1:244914242..244914444hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg38203
hg19203
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5562975
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16897705
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.004215


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