A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037931



Internal ID19127150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:19811063..19947463hg38UCSC Ensembl
Innerchr15:20016316..20152716hg19UCSC Ensembl
Innerchr15:18276329..18412730hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38136401
hg19136401
hg18136402
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2170n100
Supporting Variantsnssv3715666, nssv3715673, nssv3715679, nssv3715667, nssv3534410, nssv3534409, nssv3715671, nssv3715662, nssv3714553, nssv3534408, nssv3715670, nssv3715674, nssv3715676, nssv3715681, nssv3715683, nssv3715672, nssv3715668, nssv3715661, nssv3534407, nssv3715682, nssv3715665, nssv3714552, nssv3715675, nssv3715664, nssv3715663, nssv3534411, nssv3715677, nssv3715684, nssv3715680, nssv3715678, nssv3715669
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)nsv1037931
Frequency
Sample Size11257
Observed Gain31
Observed Loss0
Observed Complex0
Frequencyn/a


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