A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv710153



Internal ID16004109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:12839881..12857981hg38UCSC Ensembl
Innerchr1:12899734..12917836hg19UCSC Ensembl
Innerchr1:12822321..12840423hg18UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3818101
hg1918103
hg1818103
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv545509
Supporting Variants
Samples
Known GenesHNRNPCL1, LOC649330, PRAMEF2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv710153
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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