A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6372440



Internal ID21029993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:14978706..14979082hg38UCSC Ensembl
chr3:15020213..15020589hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg38377
hg19377
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18096335
Samples
Known GenesNR2C2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6372440
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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