A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14038430



Internal ID21168222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:220817559..220817623hg38UCSC Ensembl
chr1:220990901..220990965hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3062941
Supporting Variants
SamplesNA12878
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)nssv14038430
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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