A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6607268



Internal ID20980339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:146868438..146875889hg38UCSC Ensembl
chr6:147189574..147197025hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg387452
hg197452
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18139083
Samples
Known GenesSTXBP5-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6607268
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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