A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6033136



Internal ID21942479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40037522..40037609hg38UCSC Ensembl
chr15:40329723..40329810hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17614054
Samples
Known GenesSRP14
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6033136
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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