A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17373883



Internal ID22599552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:3618543..3631080hg38UCSC Ensembl
chr17:3521837..3534374hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3812538
hg1912538
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5927855
Supporting Variants
Samples
Known GenesSHPK
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17373883
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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