A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5870049



Internal ID22644984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:46449242..46449413hg38UCSC Ensembl
chr1:46914914..46915085hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg38172
hg19172
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17383752
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5870049
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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