A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6076408



Internal ID21985641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:6659308..6659308hg38UCSC Ensembl
chr5:6659421..6659421hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17543861
Samples
Known GenesSRD5A1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6076408
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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