A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv913838



Internal ID15861108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:87815738..88850700hg38UCSC Ensembl
Innerchr2:88115257..89150213hg19UCSC Ensembl
Innerchr2:87896372..88931328hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg381034963
hg191034957
hg181034957
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv582381
Supporting Variants
Samples
Known GenesANKRD36BP2, EIF2AK3, FABP1, FOXI3, KRCC1, MIR4436A, MIR4780, RGPD1, RGPD2, RPIA, SMYD1, TEX37, THNSL2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv913838
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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