A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1118173



Internal ID18934203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:47482962..47504919hg38UCSC Ensembl
Outerchr10:48234400..48256400hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3821958
hg1922001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3980840
SamplesKWS1
Known GenesAGAP9, ANXA8, FAM25C, FAM25G
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1118173
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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