A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv616005



Internal ID16056728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:137036493..137173890hg38UCSC Ensembl
Innerchr9:139930945..140068342hg19UCSC Ensembl
Innerchr9:139050766..139188163hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38137398
hg19137398
hg18137398
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1148359
Samples
Known GenesC9orf139, DPP7, ENTPD2, GRIN1, LRRC26, MAN1B1, MAN1B1-AS1, MIR3621, NPDC1, SAPCD2, TMEM210, UAP1L1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv616005
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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