A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6140558



Internal ID339751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:139953659..139959659hg38UCSC Ensembl
chr5:139333244..139339244hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg386001
hg196001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16974446
Samples
Known GenesNRG2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6140558
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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