A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6405566



Internal ID21063119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:149036101..149038300hg38UCSC Ensembl
chr5:148415664..148417863hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg382200
hg192200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18126532
Samples
Known GenesSH3TC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6405566
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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