A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6607602



Internal ID20980673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:136475795..136476543hg38UCSC Ensembl
chr6:136796933..136797681hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg38749
hg19749
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18140129
Samples
Known GenesMAP7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6607602
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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