A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5926984



Internal ID22702212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:139147288..139148202hg38UCSC Ensembl
chr7:138832034..138832948hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38915
hg19915
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17441380
Samples
Known GenesTTC26
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5926984
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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