A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6407560



Internal ID21065113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:132997079..133006905hg38UCSC Ensembl
chr5:132332771..132342597hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg389827
hg199827
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18127156
Samples
Known GenesZCCHC10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6407560
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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