A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6615033



Internal ID20988104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:138527139..138527879hg38UCSC Ensembl
chr6:138848276..138849016hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg38741
hg19741
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18138392
Samples
Known GenesNHSL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6615033
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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