A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5876503



Internal ID22651464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:5539918..5540024hg38UCSC Ensembl
chr2:5680050..5680156hg19UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17398593
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5876503
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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