A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6412357



Internal ID21069910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:102265535..102277397hg38UCSC Ensembl
chr5:101601239..101613101hg19UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg3811863
hg1911863
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18122070
Samples
Known GenesSLCO4C1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6412357
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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