A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6401180



Internal ID21058733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:94375727..94376486hg38UCSC Ensembl
chr5:93711432..93712191hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38760
hg19760
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18136454
Samples
Known GenesKIAA0825
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6401180
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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