A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6356538



Internal ID21014091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:15117701..15571300hg38UCSC Ensembl
chr4:15119325..15572923hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg38453600
hg19453599
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212095
Samples
Known GenesC1QTNF7, CC2D2A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6356538
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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