A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18209440



Internal ID20776480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:101801849..101817170hg38UCSC Ensembl
chr4:102723006..102738327hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3815322
hg1915322
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6383788
Supporting Variants
Samples
Known GenesBANK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18209440
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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