A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6406400



Internal ID21063953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:7347001..7350700hg38UCSC Ensembl
chr6:7347234..7350933hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg383700
hg193700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18147498
Samples
Known GenesCAGE1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6406400
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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