A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6363235



Internal ID21020788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:47426662..47441095hg38UCSC Ensembl
chr3:47468152..47482585hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3814434
hg1914434
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18100753
Samples
Known GenesSCAP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6363235
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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