A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3054626



Internal ID21186589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:7300262..7300347hg38UCSC Ensembl
chr5:7300375..7300460hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14018039
SamplesNA12878
Known GenesLOC442132
MethodSequencing
AnalysisCombines the NGS (e.g., Illumina) and SMS (e.g., Pacbio) for detecting large and small SVs (parameters the same as commit eee31f6 of https://bitbucket.org/xianfan/hybridassemblysv)
Platform
Comments
ReferenceFan_et_al_2017
Pubmed ID28104618
Accession Number(s)nsv3054626
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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