A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3980855



Internal ID19203571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:122374384..122375084hg38UCSC Ensembl
Outerchr10:124133900..124134600hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38701
hg19701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1118188
Supporting Variants
SamplesKWS1
Known GenesPLEKHA1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3980855
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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