A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14021956



Internal ID21172334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:9998493..9998493hg38UCSC Ensembl
chr2:10138621..10138621hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg38166
hg19166
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3044894
Supporting Variants
SamplesNA12878
Known GenesGRHL1
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)nssv14021956
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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