A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6037389



Internal ID21946732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:48270743..48270840hg38UCSC Ensembl
chr15:48562940..48563037hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17600356
Samples
Known GenesSLC12A1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6037389
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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