A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6403222



Internal ID21060775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:10465448..10718419hg38UCSC Ensembl
chr6:10465681..10718652hg19UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg38252972
hg19252972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18134650
Samples
Known GenesC6orf52, GCNT2, PAK1IP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6403222
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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