A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18154082



Internal ID20721122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:131242051..131243511hg38UCSC Ensembl
chr7:130926810..130928270hg19UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg381461
hg191461
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6433614
Supporting Variants
Samples
Known GenesMKLN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18154082
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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