A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001544



Internal ID18744075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:175709801..175798369hg38UCSC Ensembl
Innerchr3:175427589..175516157hg19UCSC Ensembl
Innerchr3:176910283..176998851hg18UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg3888569
hg1988569
hg1888569
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3613625
Samples
Known GenesNAALADL2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1001544
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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