A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6607299



Internal ID20980370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:100086101..100087747hg38UCSC Ensembl
chr7:99683724..99685370hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg381647
hg191647
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18147678
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6607299
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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