A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16961982



Internal ID41951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:7264025..7269328hg38UCSC Ensembl
chr5:7264138..7269441hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg385304
hg195304
Variant TypeCNV mobile element deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6147432
Supporting Variants
Samples
Known GenesMIR4454
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16961982
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.006869


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