A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6380789



Internal ID21038342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:84493001..84493500hg38UCSC Ensembl
chr4:85414154..85414653hg19UCSC Ensembl
Cytoband4q21.23
Allele length
AssemblyAllele length
hg38500
hg19500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18119639
Samples
Known GenesNKX6-1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6380789
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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