A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6403337



Internal ID21060890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:36727055..36729737hg38UCSC Ensembl
chr6:36694832..36697514hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg382683
hg192683
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18141772
Samples
Known GenesRAB44
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6403337
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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