A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6614799



Internal ID20987870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:6469203..6469525hg38UCSC Ensembl
chr7:6508834..6509156hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18158586
Samples
Known GenesKDELR2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6614799
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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