A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6409547



Internal ID21067100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:56467078..56481589hg38UCSC Ensembl
chr5:55762905..55777416hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3814512
hg1914512
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18131806
Samples
Known GenesLOC102467147
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6409547
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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