A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999607



Internal ID19159144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:51869171..52036024hg38UCSC Ensembl
Innerchr2:52096309..52263162hg19UCSC Ensembl
Innerchr2:51949813..52116666hg18UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg38166854
hg19166854
hg18166854
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3816n100
Supporting Variantsnssv3726028
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv999607
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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