A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17383952



Internal ID22441822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:63596355..63599597hg38UCSC Ensembl
chr17:61673714..61676956hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg383243
hg193243
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5939691
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17383952
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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