A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6615710



Internal ID20988781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:71130101..71133400hg38UCSC Ensembl
chr7:70595087..70598386hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg383300
hg193300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223712
Samples
Known GenesWBSCR17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6615710
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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