A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17473059



Internal ID22530951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:29855070..29864446hg38UCSC Ensembl
chr17:28182088..28191464hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg389377
hg199377
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5878674
Supporting Variants
Samples
Known GenesSSH2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17473059
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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