A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv710022



Internal ID15657292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:12687857..12727665hg38UCSC Ensembl
Innerchr1:12747871..12787632hg19UCSC Ensembl
Innerchr1:12670458..12710219hg18UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3839809
hg1939762
hg1839762
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv545444
Supporting Variants
Samples
Known GenesAADACL3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv710022
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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