A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6369574



Internal ID21027127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:63843528..63853645hg38UCSC Ensembl
chr3:63829204..63839321hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3810118
hg1910118
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18101464
Samples
Known GenesC3orf49, THOC7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6369574
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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