A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16952077



Internal ID35409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:70093000..70216000hg38UCSC Ensembl
chr4:70958717..71081717hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg38123001
hg19123001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5458924
Supporting Variants
Samples
Known GenesC4orf40, CSN1S2BP, ODAM
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16952077
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000781


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