A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3729244



Internal ID19027525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:141409668..141477739hg38UCSC Ensembl
Innerchr2:142167237..142235308hg19UCSC Ensembl
Innerchr2:141883707..141951778hg18UCSC Ensembl
Cytoband2q22.1
Allele length
AssemblyAllele length
hg3868072
hg1968072
hg1868072
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1002208
Supporting Variants
Samples
Known GenesLRP1B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3729244
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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