A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6423757



Internal ID21081310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:144611004..144615237hg38UCSC Ensembl
chr7:144308097..144312330hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg384234
hg194234
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18153125
Samples
Known GenesTPK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6423757
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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