A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6361038



Internal ID21018591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:27388822..27388913hg38UCSC Ensembl
chr3:27430313..27430404hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18101905
Samples
Known GenesSLC4A7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6361038
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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