A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17382064



Internal ID22439934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:5808100..5856176hg38UCSC Ensembl
chr17:5711420..5759496hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3848077
hg1948077
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5931347
Supporting Variants
Samples
Known GenesLOC339166
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17382064
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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