A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6362020



Internal ID21019573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:3077629..3078860hg38UCSC Ensembl
chr4:3079356..3080587hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg381232
hg191232
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18114773
Samples
Known GenesHTT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6362020
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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