A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6611581



Internal ID20984652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99589701..99598900hg38UCSC Ensembl
chr7:99187324..99196523hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg389200
hg199200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18162435
Samples
Known GenesLOC100289187
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6611581
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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