A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5887073



Internal ID22662064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:29736184..29751339hg38UCSC Ensembl
chr17:28063202..28078357hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3815156
hg1915156
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17473055
Samples
Known GenesSSH2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5887073
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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