A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6415629



Internal ID21073182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:149123648..149129030hg38UCSC Ensembl
chr7:148820740..148826122hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg385383
hg195383
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18237003
Samples
Known GenesZNF398, ZNF425
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6415629
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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