A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6601788



Internal ID20974859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:157405400..157410903hg38UCSC Ensembl
chr6:157826432..157831935hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg385504
hg195504
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216700
Samples
Known GenesZDHHC14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6601788
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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