A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6601124



Internal ID20974195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:12247951..12358103hg38UCSC Ensembl
chr7:12287577..12397729hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38110153
hg19110153
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18151879
Samples
Known GenesVWDE
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6601124
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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