A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5874951



Internal ID22649905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:29772390..29779457hg38UCSC Ensembl
chr17:28099408..28106475hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg387068
hg197068
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17477557
Samples
Known GenesSSH2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5874951
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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