A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6420639



Internal ID21078192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:91301601..91302600hg38UCSC Ensembl
chr8:92313829..92314828hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18172766
Samples
Known GenesSLC26A7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6420639
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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