A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003168



Internal ID19092386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:4155585..4175565hg38UCSC Ensembl
Innerchr2:4203175..4223155hg19UCSC Ensembl
Innerchr2:4181050..4201030hg18UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3819981
hg1919981
hg1819981
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3704n100
Supporting Variantsnssv3571310, nssv3571313, nssv3571312, nssv3571315, nssv3571311, nssv3571308, nssv3571314, nssv3571309
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)nsv1003168
Frequency
Sample Size11257
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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