A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv921607



Internal ID15868877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:153804735..153880157hg38UCSC Ensembl
Innerchr2:154661248..154736670hg19UCSC Ensembl
Innerchr2:154369494..154444916hg18UCSC Ensembl
Cytoband2q23.3
Allele length
AssemblyAllele length
hg3875423
hg1975423
hg1875423
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv583366
Supporting Variants
Samples
Known GenesGALNT13
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv921607
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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