A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011632



Internal ID19100849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:15703..115348hg38UCSC Ensembl
Innerchr2:15703..115348hg19UCSC Ensembl
Innerchr2:5703..105348hg18UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3899646
hg1999646
hg1899646
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3692n100
Supporting Variantsnssv3571241, nssv3571240, nssv3571242, nssv3571239
Samples
Known GenesFAM110C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1011632
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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