A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1110503



Internal ID19254585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:156982006..156983606hg38UCSC Ensembl
Outerchr7:156774700..156776300hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg381601
hg191601
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3721n106
Supporting Variantsnssv3960155
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1110503
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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