A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6382930



Internal ID21040483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:5472456..5472988hg38UCSC Ensembl
chr5:5472569..5473101hg19UCSC Ensembl
Cytoband5p15.32
Allele length
AssemblyAllele length
hg38533
hg19533
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18131709
Samples
Known GenesKIAA0947
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6382930
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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