A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2758070



Internal ID17830904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:175359852..175370396hg38UCSC Ensembl
Innerchr3:175077641..175088185hg19UCSC Ensembl
Innerchr3:176560335..176570879hg18UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg3810545
hg1910545
hg1810545
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv965410
Supporting Variants
SamplesHGDP00998
Known GenesMIR4789, NAALADL2
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2758070
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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