A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18212020



Internal ID20779060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:145932595..146233198hg38UCSC Ensembl
chr4:146853747..147154350hg19UCSC Ensembl
Cytoband4q31.22
Allele length
AssemblyAllele length
hg38300604
hg19300604
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6386890
Supporting Variants
Samples
Known GenesLINC01095, LSM6, ZNF827
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18212020
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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