A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17382287



Internal ID22440157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:73190134..73190219hg38UCSC Ensembl
chr17:71186273..71186358hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5938480
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17382287
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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