A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17712149



Internal ID135815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:21185566..21185634hg38UCSC Ensembl
chr17:21088879..21088947hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5533111
Supporting Variants
Samples
Known GenesDHRS7B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17712149
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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