A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6396103



Internal ID21053656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:54161101..54161900hg38UCSC Ensembl
chr6:54025899..54026698hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18144716
Samples
Known GenesMLIP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6396103
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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