A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6619660



Internal ID20992731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99968693..99976035hg38UCSC Ensembl
chr7:99566316..99573658hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg387343
hg197343
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18162461
Samples
Known GenesAZGP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6619660
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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