A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010091



Internal ID19099310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:130073920..130109235hg38UCSC Ensembl
Innerchr3:129792763..129828078hg19UCSC Ensembl
Innerchr3:131275453..131310768hg18UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3835316
hg1935316
hg1835316
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4899n100
Supporting Variantsnssv3607126
Samples
Known GenesALG1L2, FAM86HP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1010091
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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