A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6390644



Internal ID21048197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:92835298..92835665hg38UCSC Ensembl
chr4:93756449..93756816hg19UCSC Ensembl
Cytoband4q22.2
Allele length
AssemblyAllele length
hg38368
hg19368
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18119765
Samples
Known GenesGRID2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6390644
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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