A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6419432



Internal ID21076985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:129681733..129681921hg38UCSC Ensembl
chr7:129321573..129321761hg19UCSC Ensembl
Cytoband7q32.2
Allele length
AssemblyAllele length
hg38189
hg19189
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18153379
Samples
Known GenesNRF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6419432
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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