A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6617210



Internal ID20990281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:98285014..98286084hg38UCSC Ensembl
chr7:97914326..97915396hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg381071
hg191071
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18161258
Samples
Known GenesBRI3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6617210
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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