A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5867607



Internal ID22642542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:30551407..30575795hg38UCSC Ensembl
chr17:28878425..28902813hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3824389
hg1924389
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17477573
Samples
Known GenesTBC1D29
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5867607
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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