A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6326571



Internal ID20859708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:98693420..98845808hg38UCSC Ensembl
chr1:99158976..99311364hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg38152389
hg19152389
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202134
Samples
Known GenesSNX7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6326571
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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