A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6397710



Internal ID21055263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:36528121..36533044hg38UCSC Ensembl
chr6:36495898..36500821hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg384924
hg194924
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18141761
Samples
Known GenesSTK38
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6397710
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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