A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16978984



Internal ID53365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:10922237..10922288hg38UCSC Ensembl
chr6:10922470..10922521hg19UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5461484
Supporting Variants
Samples
Known GenesSYCP2L
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16978984
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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