A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6405546



Internal ID21063099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:112974794..113079100hg38UCSC Ensembl
chr5:112310491..112414797hg19UCSC Ensembl
Cytoband5q22.2
Allele length
AssemblyAllele length
hg38104307
hg19104307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18123113
Samples
Known GenesDCP2, MCC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6405546
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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