A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6604915



Internal ID20977986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:126406230..126432079hg38UCSC Ensembl
chr6:126727376..126753225hg19UCSC Ensembl
Cytoband6q22.32
Allele length
AssemblyAllele length
hg3825850
hg1925850
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18138747
Samples
Known GenesCENPW
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6604915
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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