A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011639



Internal ID19100856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:89896137..90079966hg38UCSC Ensembl
Innerchr2:89934947..90118808hg19UCSC Ensembl
Innerchr2:89571989..89756113hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38183830
hg19183862
hg18184125
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3972n100
Supporting Variantsnssv3579795, nssv3579791, nssv3579792, nssv3579796, nssv3579794, nssv3579793
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)nsv1011639
Frequency
Sample Size11257
Observed Gain1
Observed Loss5
Observed Complex0
Frequencyn/a


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