A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6612705



Internal ID20985776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:143874201..143878700hg38UCSC Ensembl
chr6:144195338..144199837hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg384500
hg194500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18140256
Samples
Known GenesZC2HC1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6612705
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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