A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17384675



Internal ID22442545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:18048004..18048298hg38UCSC Ensembl
chr17:17951318..17951612hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38295
hg19295
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5929659
Supporting Variants
Samples
Known GenesGID4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17384675
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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