A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5937670



Internal ID22713041
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 StatusM
Merged Variants
Supporting Variantsnssv17377161
Samples
Known GenesFAM27L, FLJ36000, MTRNR2L1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5937670
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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