A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6399601



Internal ID21057154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:139945401..139947300hg38UCSC Ensembl
chr5:139324986..139326885hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18126001
Samples
Known GenesNRG2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6399601
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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