A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6429756



Internal ID21087309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:144737491..144799116hg38UCSC Ensembl
chr7:144434584..144496209hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3861626
hg1961626
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18153139
Samples
Known GenesTPK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6429756
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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