A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6606976



Internal ID20980047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:17912883..17922642hg38UCSC Ensembl
chr7:17952506..17962265hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg389760
hg199760
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18154775
Samples
Known GenesSNX13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6606976
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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