A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3050757



Internal ID21182807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:135549015..135549078hg38UCSC Ensembl
chr9:138440861..138440924hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14022273
SamplesNA12878
Known GenesOBP2A
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)nsv3050757
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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