A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18207634



Internal ID20774674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:127607869..127631583hg38UCSC Ensembl
chr2:128365444..128389158hg19UCSC Ensembl
Cytoband2q14.3
Allele length
AssemblyAllele length
hg3823715
hg1923715
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6343457
Supporting Variants
Samples
Known GenesMYO7B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18207634
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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