A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6606149



Internal ID20979220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:97298301..97301100hg38UCSC Ensembl
chr7:96927613..96930412hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg382800
hg192800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18160791
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6606149
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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