A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1117581



Internal ID19265975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:133009437..133009499hg38UCSC Ensembl
Outerchr5:132345129..132345191hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3956893
SamplesKWS1
Known GenesZCCHC10
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1117581
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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