A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5868042



Internal ID22642977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:151181321..151182110hg38UCSC Ensembl
chr1:151153797..151154586hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38790
hg19790
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17351781
Samples
Known GenesVPS72
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5868042
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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