A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6398302



Internal ID21055855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:57003767..57005671hg38UCSC Ensembl
chr6:56868565..56870469hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg381905
hg191905
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18146577
Samples
Known GenesBEND6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6398302
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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