A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6325006



Internal ID20858136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:40533601..40715200hg38UCSC Ensembl
chr1:40999273..41180872hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg38181600
hg19181600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203101
Samples
Known GenesNFYC, NFYC-AS1, RIMS3, ZNF684
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6325006
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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