A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5986897



Internal ID21896240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:173278328..173278689hg38UCSC Ensembl
chr2:174143056..174143417hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg38362
hg19362
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17517904
Samples
Known GenesMLK7-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5986897
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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