A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17473752



Internal ID22531645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:40653821..40658786hg38UCSC Ensembl
chr17:38810073..38815038hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg384966
hg194966
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5872438
Supporting Variants
Samples
Known GenesKRT222
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17473752
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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