A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6332483



Internal ID20865655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:216750656..216751366hg38UCSC Ensembl
chr1:216923998..216924708hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg38711
hg19711
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18057540
Samples
Known GenesESRRG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6332483
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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