A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17377732



Internal ID22435602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:44170873..44170934hg38UCSC Ensembl
chr17:42248241..42248302hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5930573
Supporting Variants
Samples
Known GenesASB16
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17377732
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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