A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6412497



Internal ID21070050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:135236201..135238300hg38UCSC Ensembl
chr5:134571891..134573990hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg382100
hg192100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18127267
Samples
Known GenesC5orf66, LOC340073
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6412497
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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