A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999822



Internal ID19159358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:76767413..76795636hg38UCSC Ensembl
Innerchr2:76994539..77022762hg19UCSC Ensembl
Innerchr2:76848047..76876270hg18UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3828224
hg1928224
hg1828224
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3582050
Samples
Known GenesLRRTM4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv999822
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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