A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6401677



Internal ID21059230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:45177513..45318065hg38UCSC Ensembl
chr6:45145250..45285802hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38140553
hg19140553
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18144144
Samples
Known GenesMIR586, SUPT3H
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6401677
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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