A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1133586



Internal ID18933453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:74415583..74457483hg38UCSC Ensembl
Outerchr4:75281300..75323200hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg3841901
hg1941901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2829n106
Supporting Variantsnssv3969150
SamplesKWS2
Known GenesAREG
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1133586
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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