A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1128218



Internal ID18937479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:8427838..8427904hg38UCSC Ensembl
Outerchr6:8428071..8428137hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3958461
SamplesKWS1
Known GenesSLC35B3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1128218
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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