A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5416018



Internal ID195261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:77887204..77887503hg38UCSC Ensembl
chr1:78352889..78353188hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38300
hg19300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16905405
Samples
Known GenesNEXN-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5416018
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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