A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6322255



Internal ID20855366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:63533743..63534220hg38UCSC Ensembl
chr1:63999414..63999891hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38478
hg19478
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18062303
Samples
Known GenesEFCAB7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6322255
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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