A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6605843



Internal ID20978914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:56447811..56624522hg38UCSC Ensembl
chr7:56515504..56692215hg19UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg38176712
hg19176712
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219871
Samples
Known GenesDKFZp434L192, LOC100240728, LOC101928401, LOC650226
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6605843
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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