A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14037000



Internal ID21167296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:59218743..59218810hg38UCSC Ensembl
chr10:60978503..60978570hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3064126
Supporting Variants
SamplesNA12878
Known GenesPHYHIPL
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)nssv14037000
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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