A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6403516



Internal ID21061069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:147830392..147830749hg38UCSC Ensembl
chr5:147209955..147210312hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg38358
hg19358
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18126145
Samples
Known GenesSPINK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6403516
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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