A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6610262



Internal ID20983333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:135860874..135861308hg38UCSC Ensembl
chr6:136182012..136182446hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg38435
hg19435
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18139524
Samples
Known GenesPDE7B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6610262
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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