A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5885084



Internal ID22660068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:187963420..187963990hg38UCSC Ensembl
chr1:187932551..187933121hg19UCSC Ensembl
Cytoband1q31.1
Allele length
AssemblyAllele length
hg38571
hg19571
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17362969
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5885084
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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