A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5896765



Internal ID22671860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:157455008..157465990hg38UCSC Ensembl
chr6:157876040..157887022hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3810983
hg1910983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17419908
Samples
Known GenesZDHHC14
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5896765
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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