A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6431643



Internal ID21089196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:131177273..131180420hg38UCSC Ensembl
chr7:130862032..130865179hg19UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg383148
hg193148
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18154073
Samples
Known GenesMKLN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6431643
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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