A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17374002



Internal ID22599671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:78111873..78111949hg38UCSC Ensembl
chr17:76107954..76108030hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5938535
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17374002
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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