A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv710497



Internal ID16004453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:15018440..15051191hg38UCSC Ensembl
Innerchr1:15344936..15377687hg19UCSC Ensembl
Innerchr1:15217523..15250274hg18UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3832752
hg1932752
hg1832752
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv545592
Supporting Variants
Samples
Known GenesKAZN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv710497
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