A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6087383



Internal ID21996616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64952176..64952176hg38UCSC Ensembl
chr15:65244454..65244454hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17612728
Samples
Known GenesANKDD1A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6087383
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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