A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6603547



Internal ID20976618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:146854839..146858134hg38UCSC Ensembl
chr6:147175975..147179270hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg383296
hg193296
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18139082
Samples
Known GenesSTXBP5-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6603547
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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