A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007395



Internal ID19096614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:4158085..4175565hg38UCSC Ensembl
Innerchr2:4205675..4223155hg19UCSC Ensembl
Innerchr2:4183550..4201030hg18UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3817481
hg1917481
hg1817481
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3704n100
Supporting Variantsnssv3571348, nssv3571349, nssv3726665, nssv3571338, nssv3571331, nssv3571350, nssv3571345, nssv3571342, nssv3571352, nssv3571347, nssv3726667, nssv3571351, nssv3571334, nssv3571332, nssv3726666, nssv3571344, nssv3571343, nssv3571339, nssv3571341, nssv3571355, nssv3571353, nssv3571340, nssv3571333, nssv3726668, nssv3571336, nssv3571354, nssv3571335, nssv3571346, nssv3571337
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1007395
Frequency
Sample Size11257
Observed Gain0
Observed Loss29
Observed Complex0
Frequencyn/a


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