A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6602574



Internal ID20975645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:20348289..20354568hg38UCSC Ensembl
chr7:20387912..20394191hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg386280
hg196280
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18156885
Samples
Known GenesITGB8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6602574
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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