A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv584753



Internal ID16025476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:237735347..237748227hg38UCSC Ensembl
Innerchr2:238643990..238656870hg19UCSC Ensembl
Innerchr2:238308729..238321609hg18UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg3812881
hg1912881
hg1812881
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv933707
Samples
Known GenesLRRFIP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv584753
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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