A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6605567



Internal ID20978638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:38253401..38353600hg38UCSC Ensembl
chr7:38293002..38393201hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38100200
hg19100200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6647n223
Supporting Variantsnssv18156499
Samples
Known GenesTARP, TRG-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6605567
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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