A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1137513



Internal ID19257026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:185209546..185210446hg38UCSC Ensembl
Outerchr4:186130700..186131600hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38901
hg19901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3969155, nssv3981812
SamplesKWS2, KWS1
Known GenesSNX25
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1137513
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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