A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6614262



Internal ID20987333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:132499075..132499700hg38UCSC Ensembl
chr6:132820214..132820839hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg38626
hg19626
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18139725
Samples
Known GenesSTX7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6614262
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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