A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6612198



Internal ID20985269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:96471001..96472700hg38UCSC Ensembl
chr7:96100313..96102012hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18160730
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6612198
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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