A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5867609



Internal ID22642544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:61412119..61414353hg38UCSC Ensembl
chr2:61639254..61641488hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg382235
hg192235
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17409572
Samples
Known GenesUSP34
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5867609
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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