A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999645



Internal ID19159181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:76089880..76224228hg38UCSC Ensembl
Innerchr2:76317006..76451354hg19UCSC Ensembl
Innerchr2:76170514..76304862hg18UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg38134349
hg19134349
hg18134349
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3582004
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)nsv999645
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer