A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6431926



Internal ID21089479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:131335067..131335480hg38UCSC Ensembl
chr7:131019826..131020239hg19UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg38414
hg19414
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18154091
Samples
Known GenesMKLN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6431926
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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