A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1122527



Internal ID18922620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:49319694..49319771hg38UCSC Ensembl
Outerchr10:50527739..50527816hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3970730
SamplesKWS2
Known GenesC10orf71
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1122527
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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