A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6415728



Internal ID21073281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:48627666..48629753hg38UCSC Ensembl
chr8:49540226..49542313hg19UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg382088
hg192088
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18167749
Samples
Known GenesLOC101929268
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6415728
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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