A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6611403



Internal ID20984474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:35766601..35772900hg38UCSC Ensembl
chr7:35806211..35812510hg19UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg386300
hg196300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234861
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6611403
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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