A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5906273



Internal ID22681471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:170891565..170891625hg38UCSC Ensembl
chr2:171748075..171748135hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17390381
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5906273
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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