A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18191998



Internal ID20759038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:29096849..29560911hg38UCSC Ensembl
chr10:29385778..29849840hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg38464063
hg19464063
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6443720
Supporting Variants
Samples
Known GenesLYZL1, MIR604, PTCHD3P1, SVIL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18191998
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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