A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1136856



Internal ID18938707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:55445071..55445276hg38UCSC Ensembl
Outerchr4:56311238..56311443hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38206
hg19206
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3974760
SamplesKWS2
Known GenesCLOCK
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1136856
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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