A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6453323



Internal ID21110876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:32747382..32906356hg38UCSC Ensembl
chr10:33036310..33195284hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg38158975
hg19158975
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183993
Samples
Known GenesCCDC7, ITGB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6453323
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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