A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5875192



Internal ID22650149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:64968563..64971869hg38UCSC Ensembl
chr2:65195697..65199003hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg383307
hg193307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17409569
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5875192
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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