A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv720005



Internal ID15667275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:103612150..103618643hg38UCSC Ensembl
Innerchr1:104154772..104161265hg19UCSC Ensembl
Innerchr1:103956295..103962788hg18UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg386494
hg196494
hg186494
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv547071
Supporting Variants
Samples
Known GenesAMY2A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv720005
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