A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14017691



Internal ID21169479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:152833262..152833262hg38UCSC Ensembl
chrX:152001806..152001806hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3047220
Supporting Variants
SamplesNA12878
Known GenesNSDHL
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)nssv14017691
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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