A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5421654



Internal ID200719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:27265967..27268889hg38UCSC Ensembl
chr1:27592458..27595380hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg382923
hg192923
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16900440
Samples
Known GenesWDTC1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5421654
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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