A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17388746



Internal ID22446616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:78267624..78267687hg38UCSC Ensembl
chr17:76263705..76263768hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5929930
Supporting Variants
Samples
Known GenesLOC100996291
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17388746
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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