A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14036777



Internal ID21167157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:1443786..1443853hg38UCSC Ensembl
chr2:1447558..1447625hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3063088
Supporting Variants
SamplesNA12878
Known GenesTPO
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)nssv14036777
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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