A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6611194



Internal ID20984265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:81618607..81643110hg38UCSC Ensembl
chr7:81247923..81272426hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3824504
hg1924504
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223735
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6611194
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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