A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6616401



Internal ID20989472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:14946634..15011956hg38UCSC Ensembl
chr7:14986259..15051581hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3865323
hg1965323
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18154036
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6616401
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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