A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6377932



Internal ID21035485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:10592318..10615161hg38UCSC Ensembl
chr5:10592430..10615273hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3822844
hg1922844
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18123448
Samples
Known GenesANKRD33B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6377932
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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