A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007716



Internal ID19096935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:89896137..90077966hg38UCSC Ensembl
Innerchr2:89934947..90116808hg19UCSC Ensembl
Innerchr2:89571989..89754113hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38181830
hg19181862
hg18182125
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3973n100
Supporting Variantsnssv3579789, nssv3579790, nssv3579788
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)nsv1007716
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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