A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6617877



Internal ID20990948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:147130401..147131500hg38UCSC Ensembl
chr6:147451537..147452636hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18141134
Samples
Known GenesSTXBP5-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6617877
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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