A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6375602



Internal ID21033155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:42438381..42438912hg38UCSC Ensembl
chr5:42438483..42439014hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg38532
hg19532
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18130450
Samples
Known GenesGHR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6375602
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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