A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1122085



Internal ID18913888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:38663479..38665179hg38UCSC Ensembl
Outerchr4:38665100..38666800hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg381701
hg191701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3969522
SamplesKWS2
Known GenesFLJ13197, KLF3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1122085
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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