A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14027209



Internal ID21160736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:77725431..77725431hg38UCSC Ensembl
chr7:77354748..77354748hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3051094
Supporting Variants
SamplesNA12878
Known GenesRSBN1L
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)nssv14027209
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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