A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3985428



Internal ID19211097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:17358666..17358741hg38UCSC Ensembl
Outerchr10:17400665..17400740hg19UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1127090
Supporting Variants
SamplesKWS1
Known GenesST8SIA6
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3985428
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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