A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6371378



Internal ID21028931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:27454405..27455513hg38UCSC Ensembl
chr3:27495896..27497004hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg381109
hg191109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18101911
Samples
Known GenesSLC4A7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6371378
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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