A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6618296



Internal ID20991367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:113741299..113748241hg38UCSC Ensembl
chr7:113381354..113388296hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg386943
hg196943
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18153484
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6618296
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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