A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6607879



Internal ID20980950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:15646501..15647200hg38UCSC Ensembl
chr7:15686126..15686825hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg38700
hg19700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18151453
Samples
Known GenesMEOX2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6607879
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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