A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv980092



Internal ID18615292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:177265741..177280395hg38UCSC Ensembl
Innerchr3:176983529..176998183hg19UCSC Ensembl
Innerchr3:178466223..178480877hg18UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg3814655
hg1914655
hg1814655
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2759361
SamplesHGDP01307
Known Genes
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv980092
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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