A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6605218



Internal ID20978289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:7276989..7466311hg38UCSC Ensembl
chr7:7316620..7505942hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38189323
hg19189323
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18159408
Samples
Known GenesCOL28A1, LOC101927354
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6605218
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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