A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6385624



Internal ID21043177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:34849201..34849800hg38UCSC Ensembl
chr5:34849306..34849905hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg38600
hg19600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18129742
Samples
Known GenesTTC23L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6385624
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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