A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv744344



Internal ID16038300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:20538176..20565668hg38UCSC Ensembl
Innerchr10:20827105..20854597hg19UCSC Ensembl
Innerchr10:20867111..20894603hg18UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3827493
hg1927493
hg1827493
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550159
Supporting Variants
Samples
Known GenesMIR4675
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv744344
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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