A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6604413



Internal ID20977484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:3783494..3798602hg38UCSC Ensembl
chr7:3823126..3838234hg19UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg3815109
hg1915109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18156446
Samples
Known GenesSDK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6604413
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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