A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14030899



Internal ID21160652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:210905858..210905928hg38UCSC Ensembl
chr2:211770582..211770652hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3059384
Supporting Variants
SamplesCHM1
Known Genes
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)nssv14030899
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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