A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6386100



Internal ID21043653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:111969713..112164894hg38UCSC Ensembl
chr4:112890869..113086050hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg38195182
hg19195182
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18105602
Samples
Known GenesC4orf32
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6386100
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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