A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17497653



Internal ID22555587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:170274428..170290801hg38UCSC Ensembl
chr5:169701432..169717805hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg3816374
hg1916374
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5842175
Supporting Variants
Samples
Known GenesLCP2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17497653
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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