A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6533255



Internal ID20906616
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 StatusM
Merged Variants
Supporting Variantsnssv18177436
Samples
Known GenesITGB4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6533255
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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