A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014145



Internal ID19103365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:14901762..14937730hg38UCSC Ensembl
Innerchr2:15041886..15077854hg19UCSC Ensembl
Innerchr2:14959337..14995305hg18UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3835969
hg1935969
hg1835969
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3577111
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)nsv1014145
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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