A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6378782



Internal ID21036335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:153395713..154001208hg38UCSC Ensembl
chr4:154316865..154922360hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg38605496
hg19605496
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212113
Samples
Known GenesKIAA0922, MND1, RNF175, SFRP2, TLR2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6378782
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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