A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6396351



Internal ID21053904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:36431445..36433870hg38UCSC Ensembl
chr6:36399222..36401647hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg382426
hg192426
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18141752
Samples
Known GenesPXT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6396351
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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