A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6420912



Internal ID21078465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:14362656..14513879hg38UCSC Ensembl
chr8:14220165..14371388hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38151224
hg19151224
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7276n223
Supporting Variantsnssv18165488
Samples
Known GenesSGCZ
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6420912
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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