A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17098375



Internal ID21500210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:63541418..63541578hg38UCSC Ensembl
chr17:61618779..61618939hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg38161
hg19161
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5603759
Supporting Variants
SamplesNA19239
Known GenesKCNH6
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17098375
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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