A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4736979



Internal ID20512934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:122124175..122124270hg38UCSC Ensembl
chr12:122608722..122608817hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16277181
Samples
Known GenesMLXIP
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4736979
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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