A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3967347



Internal ID19243671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:6909573..6910473hg38UCSC Ensembl
Outerchr4:6911300..6912200hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg38901
hg19901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1112849
Supporting Variants
SamplesKWS2
Known GenesTBC1D14
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3967347
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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