A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6375131



Internal ID21032684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:71750301..71755400hg38UCSC Ensembl
chr3:71799452..71804551hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg385100
hg195100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18103764
Samples
Known GenesEIF4E3, GPR27
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6375131
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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