A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3049036



Internal ID21181084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41311817..41311991hg38UCSC Ensembl
chr15:41604015..41604189hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38175
hg19175
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14021232
SamplesNA12878
Known GenesOIP5
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)nsv3049036
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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