A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6322088



Internal ID20855197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:40696422..40699390hg38UCSC Ensembl
chr1:41162094..41165062hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg382969
hg192969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18060776
Samples
Known GenesNFYC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6322088
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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