A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16903505



Internal ID3147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:29671969..30538747hg38UCSC Ensembl
chr1:30144816..31011594hg19UCSC Ensembl
Cytoband1p35.2
Allele length
AssemblyAllele length
hg38866779
hg19866779
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6147122
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16903505
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.003278


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