A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5886441



Internal ID22661428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:61481559..61481847hg38UCSC Ensembl
chr2:61708694..61708982hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg38289
hg19289
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17407573
Samples
Known GenesXPO1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5886441
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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