A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6607337



Internal ID20980408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:7690245..7704002hg38UCSC Ensembl
chr7:7729876..7743633hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3813758
hg1913758
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18158332
Samples
Known GenesRPA3, RPA3-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6607337
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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