A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6032470



Internal ID21941813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:27003842..27003969hg38UCSC Ensembl
chr15:27248989..27249116hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17612535
Samples
Known GenesGABRG3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6032470
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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