A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6601719



Internal ID20974790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:135952264..135952701hg38UCSC Ensembl
chr6:136273402..136273839hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg38438
hg19438
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18139533
Samples
Known GenesPDE7B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6601719
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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