A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18231721



Internal ID20798761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:69587201..69597900hg38UCSC Ensembl
chr7:69052187..69062886hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg3810700
hg1910700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6614104
Supporting Variants
Samples
Known GenesLOC100507468
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18231721
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00059


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