A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3966878



Internal ID18886221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:114313446..114313758hg38UCSC Ensembl
Outerchr7:113953501..113953813hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1121386
Supporting Variants
SamplesKWS2
Known GenesFOXP2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3966878
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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