A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046413



Internal ID19135632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:22572335..23121986hg38UCSC Ensembl
Innerchr15:22751082..23300761hg19UCSC Ensembl
Innerchr15:20302446..20852202hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38549652
hg19549680
hg18549757
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2405n100
Supporting Variantsnssv3715538, nssv3538863, nssv3538864, nssv3538866, nssv3538865, nssv3715537, nssv3715535, nssv3715534, nssv3715536
Samples
Known GenesCYFIP1, GOLGA8I, HERC2P2, LOC283683, NIPA1, NIPA2, TUBGCP5, WHAMMP3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046413
Frequency
Sample Size11257
Observed Gain5
Observed Loss4
Observed Complex0
Frequencyn/a


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