A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5852622



Internal ID22627557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:9606770..9608189hg38UCSC Ensembl
chr12:9759366..9760785hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg381420
hg191420
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17468219, nssv17455318
Samples
Known GenesKLRB1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5852622
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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