A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3003034



Internal ID17295986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:139990032..139990731hg38UCSC Ensembl
Outerchr2:140747601..140748300hg19UCSC Ensembl
Cytoband2q22.1
Allele length
AssemblyAllele length
hg38700
hg19700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv953186
Supporting Variants
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3003034
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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