A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17476207



Internal ID22534105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:21252605..21253641hg38UCSC Ensembl
chr17:21155918..21156953hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg381037
hg191036
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5868230
Supporting Variants
Samples
Known GenesC17orf103
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17476207
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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