A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6428179



Internal ID21085732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:56536501..56550600hg38UCSC Ensembl
chr8:57449060..57463159hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg3814100
hg1914100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18169202
Samples
Known GenesLINC00968
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6428179
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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