A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14024629



Internal ID21174099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:41730128..41730128hg38UCSC Ensembl
chr17:39886380..39886380hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3058465
Supporting Variants
SamplesNA12878
Known GenesHAP1
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)nssv14024629
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer