A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1136825



Internal ID18923140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:24547880..24547943hg38UCSC Ensembl
Outerchr4:24549503..24549566hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3957466, nssv3973911
SamplesKWS2, KWS1
Known GenesDHX15
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1136825
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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