A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5867940



Internal ID22642875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:27487687..27488247hg38UCSC Ensembl
chr2:27710554..27711114hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg38561
hg19561
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17391095
Samples
Known GenesIFT172
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5867940
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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