A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18225210



Internal ID20792250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:89446569..89685111hg38UCSC Ensembl
chr6:90156288..90394830hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38238543
hg19238543
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6398915
Supporting Variants
Samples
Known GenesANKRD6, LYRM2, MDN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18225210
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0001


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