A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3001939



Internal ID17294891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:8740011..8740351hg38UCSC Ensembl
Outerchr10:8781974..8782314hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38341
hg19341
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv956895
Supporting Variants
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3001939
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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