A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv707625



Internal ID16001581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:609586..634224hg38UCSC Ensembl
Innerchr1:544966..569604hg19UCSC Ensembl
Innerchr1:534829..559467hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3824639
hg1924639
hg1824639
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv544875
Supporting Variants
Samples
Known GenesMIR6723
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv707625
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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