A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549122



Internal ID16336531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:210550081..210551435hg38UCSC Ensembl
Innerchr1:210723425..210724779hg19UCSC Ensembl
Innerchr1:208790048..208791402hg18UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg381355
hg191355
hg181355
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv736822
Samples
Known GenesHHAT
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549122
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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