A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6037819



Internal ID21947162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:47512956..47534781hg38UCSC Ensembl
chr15:47805153..47826978hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3821826
hg1921826
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17600101
Samples
Known GenesSEMA6D
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6037819
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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