A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6376737



Internal ID21034290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:99180425..99444855hg38UCSC Ensembl
chr4:100101582..100366012hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg38264431
hg19264431
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214410
Samples
Known GenesADH1A, ADH1B, ADH1C, ADH6, ADH7, LOC100507053
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6376737
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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