A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6386890



Internal ID21044443
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 StatusM
Merged Variants
Supporting Variantsnssv18212020
Samples
Known GenesLINC01095, LSM6, ZNF827
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6386890
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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