A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv708612



Internal ID16002568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:1665581..1696548hg38UCSC Ensembl
Innerchr1:1597020..1627987hg19UCSC Ensembl
Innerchr1:1586883..1617847hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3830968
hg1930968
hg1830965
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv545024
Supporting Variants
Samples
Known GenesCDK11B, SLC35E2B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv708612
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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