A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5868230



Internal ID22643165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:21252605..21253641hg38UCSC Ensembl
chr17:21155918..21156953hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg381037
hg191036
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17476207, nssv17476208
Samples
Known GenesC17orf103
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5868230
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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