A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6600374



Internal ID20973445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:136874557..136875024hg38UCSC Ensembl
chr6:137195695..137196162hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg38468
hg19468
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18138312
Samples
Known GenesPEX7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6600374
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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