A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv712652



Internal ID16006608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:41365375..41395711hg38UCSC Ensembl
Innerchr1:41831047..41861383hg19UCSC Ensembl
Innerchr1:41603634..41633970hg18UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg3830337
hg1930337
hg1830337
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv546104
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv712652
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