A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1111922



Internal ID19286803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:79187583..79187682hg38UCSC Ensembl
Outerchr14:79653926..79654025hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1107n106
Supporting Variantsnssv3989039, nssv3955078
SamplesKWS2, KWS1
Known GenesNRXN3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1111922
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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