A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041700



Internal ID19130919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135259826..135417489hg38UCSC Ensembl
Innerchr9:138151672..138309335hg19UCSC Ensembl
Innerchr9:137291493..137449156hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38157664
hg19157664
hg18157664
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7726n100
Supporting Variantsnssv3696464, nssv3696488, nssv3696475, nssv3759850, nssv3759855, nssv3696476, nssv3696474, nssv3759846, nssv3696480, nssv3696470, nssv3759845, nssv3696471, nssv3759851, nssv3759848, nssv3696481, nssv3696487, nssv3696467, nssv3759849, nssv3759847, nssv3759852, nssv3696477, nssv3696483, nssv3759853, nssv3696482, nssv3696465, nssv3696478, nssv3696469, nssv3696468, nssv3696473, nssv3696479, nssv3696466, nssv3696484, nssv3696486, nssv3696485, nssv3696472, nssv3759854
Samples
Known GenesC9orf62
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1041700
Frequency
Sample Size11257
Observed Gain36
Observed Loss0
Observed Complex0
Frequencyn/a


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