A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv956659



Internal ID16958846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:85292012..85292358hg38UCSC Ensembl
Outerchr2:85519135..85519481hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38347
hg19347
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3003828
SamplesBILGI_BIOE
Known GenesTCF7L1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv956659
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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