A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4733421



Internal ID20509351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:9606669..9606725hg38UCSC Ensembl
chr12:9759265..9759321hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16293289
Samples
Known GenesKLRB1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4733421
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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