A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3065667



Internal ID21197097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:1374131..1374365hg38UCSC Ensembl
chrX:1493024..1493258hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg38235
hg19235
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14034743
SamplesCHM1
Known GenesIL3RA
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)nsv3065667
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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