A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569004



Internal ID16009727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34426393..34579095hg38UCSC Ensembl
Innerchr15:34718594..34871296hg19UCSC Ensembl
Innerchr15:32505886..32658588hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38152703
hg19152703
hg18152703
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149127, nssv1149124, nssv1149126, nssv1149130, nssv1149118, nssv1149129, nssv1149114, nssv1149123, nssv1149122, nssv1149128, nssv1149115, nssv1149116, nssv1149121, nssv1149125, nssv1149120, nssv1149117, nssv1149119
SamplesNINDS_247, NINDS_243, NINDS_209, NINDS_80, NINDS_114, NINDS_116, NINDS_217, NINDS_110, NINDS_202, NINDS_85, NINDS_181, NINDS_199, NINDS_45, NINDS_29, NINDS_60, NINDS_245, NINDS_226
Known GenesGOLGA8A, GOLGA8B, MIR1233-1, MIR1233-2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569004
Frequency
Sample Size17421
Observed Gain3
Observed Loss14
Observed Complex0
Frequencyn/a


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