A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3968111



Internal ID18880718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:200069209..200069261hg38UCSC Ensembl
Outerchr1:200038337..200038389hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1113210
Supporting Variants
SamplesKWS2
Known GenesNR5A2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3968111
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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