A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3052778



Internal ID21184812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:26393186..26393186hg38UCSC Ensembl
chrY:28539333..28539333hg19UCSC Ensembl
CytobandYq11.23
Allele length
AssemblyAllele length
hg38525
hg19525
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14036262
SamplesNA12878
Known Genes
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)nsv3052778
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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