A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1124986



Internal ID19274632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:155957806..155959706hg38UCSC Ensembl
Outerchr7:155750500..155752400hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg381901
hg191901
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3718n106
Supporting Variantsnssv3977792
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1124986
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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