A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6425015



Internal ID21082568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:144677530..144799483hg38UCSC Ensembl
chr7:144374623..144496576hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38121954
hg19121954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18153135
Samples
Known GenesTPK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6425015
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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