A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009756



Internal ID18752287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:87094919..87747090hg38UCSC Ensembl
Innerchr2:87322042..88046609hg19UCSC Ensembl
Innerchr2:87175553..87827724hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38652172
hg19724568
hg18652172
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3889n100
Supporting Variantsnssv3582200
Samples
Known GenesLINC00152, MIR4435-1, MIR4435-2, MIR4771-1, MIR4771-2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1009756
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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