A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6619857



Internal ID20992928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:6809701..7217700hg38UCSC Ensembl
chr7:6849332..7257331hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38408000
hg19408000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6557n223
Supporting Variantsnssv18228894
Samples
Known GenesC1GALT1, CCZ1B, LOC100131257
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6619857
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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