A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6426432



Internal ID21083985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:149122069..149124292hg38UCSC Ensembl
chr7:148819161..148821384hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg382224
hg192224
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18154013
Samples
Known GenesZNF425
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6426432
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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