A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6520656



Internal ID20894017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:76709001..76710800hg38UCSC Ensembl
chr17:74705083..74706882hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197074
Samples
Known GenesMXRA7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6520656
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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