A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6361047



Internal ID21018600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:44760569..44763798hg38UCSC Ensembl
chr3:44802061..44805290hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg383230
hg193230
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18100618
Samples
Known GenesKIAA1143, KIF15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6361047
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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