A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5415681



Internal ID194933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:15085472..15091431hg38UCSC Ensembl
chr1:15411968..15417927hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg385960
hg195960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16895910
Samples
Known GenesKAZN
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5415681
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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