A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1112142



Internal ID18933504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:152068854..152071098hg38UCSC Ensembl
Outerchr6:152389989..152392233hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg382245
hg192245
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3413n106
Supporting Variantsnssv3965833
SamplesKWS2
Known GenesESR1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1112142
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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