A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14018333



Internal ID21169915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6795269..6795372hg38UCSC Ensembl
chr10:6837231..6837334hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3056439
Supporting Variants
SamplesNA12878
Known GenesLINC00707
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)nssv14018333
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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