A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6402473



Internal ID21060026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:26465174..26506396hg38UCSC Ensembl
chr6:26465402..26506624hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg3841223
hg1941223
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18140754
Samples
Known GenesBTN1A1, BTN2A1, LOC285819
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6402473
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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