A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6405464



Internal ID21063017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:76835401..76859400hg38UCSC Ensembl
chr5:76131226..76155225hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg3824000
hg1924000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18134500
Samples
Known GenesS100Z
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6405464
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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