A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016994



Internal ID19106211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:28187705..28347681hg38UCSC Ensembl
Innerchr9:28187703..28347679hg19UCSC Ensembl
Innerchr9:28177703..28337679hg18UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38159977
hg19159977
hg18159977
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7490n100
Supporting Variantsnssv3755880, nssv3692022, nssv3692024, nssv3692023
Samples
Known GenesLINGO2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1016994
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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