A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3051465



Internal ID21183517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3092652..3092807hg38UCSC Ensembl
chr6:3092886..3093041hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg38156
hg19156
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14026658
SamplesNA12878
Known GenesRIPK1
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)nsv3051465
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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