A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6617112



Internal ID20990183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:84171927..84476371hg38UCSC Ensembl
chr7:83801243..84105687hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38304445
hg19304445
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231548
Samples
Known GenesSEMA3A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6617112
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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