A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3980713



Internal ID18872566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:50077840..50241340hg38UCSC Ensembl
Outerchr10:51837600..52001100hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg38163501
hg19163501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1143508
Supporting Variants
SamplesKWS1
Known GenesASAH2, FAM21A, FAM21B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3980713
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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