A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6385710



Internal ID21043263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:77183913..77184069hg38UCSC Ensembl
chr4:78105066..78105222hg19UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg38157
hg19157
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18120295
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6385710
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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