A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6422243



Internal ID21079796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:144835401..144836000hg38UCSC Ensembl
chr7:144532494..144533093hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38600
hg19600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18153150
Samples
Known GenesTPK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6422243
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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