A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6395116



Internal ID21052669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:55828043..55828721hg38UCSC Ensembl
chr4:56694209..56694887hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38679
hg19679
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18118385
Samples
Known GenesLOC644145
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6395116
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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