A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16903149



Internal ID2921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:60774121..60781428hg38UCSC Ensembl
chr1:61239793..61247100hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg387308
hg197308
Variant TypeCNV mobile element deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6147437
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16903149
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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