A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6600902



Internal ID20973973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:119211223..119392959hg38UCSC Ensembl
chr7:118851277..119033013hg19UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg38181737
hg19181737
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18150417
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6600902
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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