A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998383



Internal ID19157919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:15382648..15496365hg38UCSC Ensembl
Innerchr2:15522772..15636489hg19UCSC Ensembl
Innerchr2:15440223..15553940hg18UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg38113718
hg19113718
hg18113718
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3577113
Samples
Known GenesNBAS
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv998383
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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