A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2997343



Internal ID17290295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:108849925..108850824hg38UCSC Ensembl
Outerchr12:109243701..109244600hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv952473
Supporting Variants
SamplesBILGI_BIOE
Known GenesSSH1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2997343
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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