A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14029916



Internal ID21162565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:92347883..92347883hg38UCSC Ensembl
chr13:93000136..93000136hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3053127
Supporting Variants
SamplesNA12878
Known GenesGPC5
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)nssv14029916
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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