A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17377161



Internal ID22435031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:22054991..22676375hg38UCSC Ensembl
chr17:21666609..22175702hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38621385
hg19509094
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5937670
Supporting Variants
Samples
Known GenesFAM27L, FLJ36000, MTRNR2L1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17377161
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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