A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17577383



Internal ID21769426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:4629042..4629042hg38UCSC Ensembl
chr6:4629276..4629276hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg38167
hg19167
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6076289
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17577383
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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