A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1124112



Internal ID19276681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:108502140..108502319hg38UCSC Ensembl
Outerchr6:108823343..108823522hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38180
hg19180
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3362n106
Supporting Variantsnssv3975425
SamplesKWS2
Known GenesLACE1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1124112
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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