A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18177436



Internal ID20744476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:75715801..75746496hg38UCSC Ensembl
chr17:73711881..73742577hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg3830696
hg1930697
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6533255
Supporting Variants
Samples
Known GenesITGB4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18177436
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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