A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17705134



Internal ID128800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90580705..90584082hg38UCSC Ensembl
chr15:91123937..91127314hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg383378
hg193378
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5526872
Supporting Variants
Samples
Known GenesCRTC3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17705134
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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