A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5923371



Internal ID22698598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:38344064..38378765hg38UCSC Ensembl
chr7:38383665..38418366hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3834702
hg1934702
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17431214
Samples
Known GenesTRG-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5923371
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer