A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6399953



Internal ID21057506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:6252151..6254158hg38UCSC Ensembl
chr6:6252384..6254391hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg382008
hg192008
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18145568
Samples
Known GenesF13A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6399953
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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