A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4738829



Internal ID20514800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:173278334..173278696hg38UCSC Ensembl
chr2:174143062..174143424hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg38363
hg19363
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16263782
Samples
Known GenesMLK7-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4738829
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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