A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6410027



Internal ID21067580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:161388098..161388540hg38UCSC Ensembl
chr5:160815104..160815546hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38443
hg19443
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18126570
Samples
Known GenesGABRB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6410027
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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