A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6378154



Internal ID21035707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:101796300..101808989hg38UCSC Ensembl
chr4:102717457..102730146hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3812690
hg1912690
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18106178
Samples
Known GenesBANK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6378154
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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