A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6376905



Internal ID21034458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:121859301..121860300hg38UCSC Ensembl
chr4:122780456..122781455hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18109013
Samples
Known GenesBBS7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6376905
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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