A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17576468



Internal ID21768511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:150386372..150386372hg38UCSC Ensembl
chr6:150707508..150707508hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6074017
Supporting Variants
Samples
Known GenesIYD
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17576468
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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