A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5892176



Internal ID22667222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:172700315..172700391hg38UCSC Ensembl
chr2:173565043..173565119hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17400713
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5892176
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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