A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6400216



Internal ID21057769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:10903312..10904855hg38UCSC Ensembl
chr6:10903545..10905088hg19UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg381544
hg191544
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18137022
Samples
Known GenesSYCP2L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6400216
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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