A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6367157



Internal ID21024710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:52975427..52976140hg38UCSC Ensembl
chr3:53009443..53010156hg19UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg38714
hg19714
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18100988
Samples
Known GenesSFMBT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6367157
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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