A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1122203



Internal ID19286618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:135457357..135457757hg38UCSC Ensembl
Outerchr8:136469600..136470000hg19UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38401
hg19401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3969646
SamplesKWS2
Known GenesKHDRBS3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1122203
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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