A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5882191



Internal ID22657168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:37807983..37808038hg38UCSC Ensembl
chr1:38273655..38273710hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17383872
Samples
Known GenesC1orf122, YRDC
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5882191
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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