A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6611868



Internal ID20984939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:113261318..113306803hg38UCSC Ensembl
chr7:112901373..112946858hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3845486
hg1945486
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18152839
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6611868
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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