A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv584752



Internal ID16025475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:237672366..237745817hg38UCSC Ensembl
Innerchr2:238581009..238654460hg19UCSC Ensembl
Innerchr2:238245748..238319199hg18UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg3873452
hg1973452
hg1873452
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv933706
Samples
Known GenesLRRFIP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv584752
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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