A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6424660



Internal ID21082213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:144560431..144566211hg38UCSC Ensembl
chr7:144257524..144263304hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg385781
hg195781
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18153118
Samples
Known GenesTPK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6424660
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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