A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17711836



Internal ID135502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:17092000..17099111hg38UCSC Ensembl
chr17:16995314..17002425hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg387112
hg197112
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6144476
Supporting Variants
Samples
Known GenesMPRIP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17711836
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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