A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3063658



Internal ID21195188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:89607808..89607934hg38UCSC Ensembl
chr6:90317527..90317653hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14035876
SamplesNA12878
Known GenesANKRD6
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)nsv3063658
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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