A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6356996



Internal ID21014549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:32351996..32352169hg38UCSC Ensembl
chr4:32353618..32353791hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38174
hg19174
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18116645
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6356996
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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