A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3989226



Internal ID18898405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:25529642..25529783hg38UCSC Ensembl
Outerchr6:25529870..25530011hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg38142
hg19142
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1112121
Supporting Variants
SamplesKWS2
Known GenesLRRC16A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3989226
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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