A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6617932



Internal ID20991003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:7821120..8019735hg38UCSC Ensembl
chr7:7860751..8059365hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38198616
hg19198615
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18158903
Samples
Known GenesGLCCI1, RPA3-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6617932
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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