A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16970822



Internal ID47882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:136239708..136239835hg38UCSC Ensembl
chr6:136560846..136560973hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5459442
Supporting Variants
Samples
Known GenesMTFR2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16970822
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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