A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6421269



Internal ID21078822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:144623366..144706480hg38UCSC Ensembl
chr7:144320459..144403573hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3883115
hg1983115
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18153128
Samples
Known GenesTPK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6421269
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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