A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027504



Internal ID19116723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:61520009..61612691hg38UCSC Ensembl
Innerchr9:44727847..44820529hg19UCSC Ensembl
Innerchr9:44667843..44760525hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3892683
hg1992683
hg1892683
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7601n100
Supporting Variantsnssv3693139, nssv3693150, nssv3693146, nssv3693151, nssv3693158, nssv3693148, nssv3693152, nssv3693136, nssv3693145, nssv3693149, nssv3693153, nssv3693155, nssv3693142, nssv3693135, nssv3693157, nssv3693143, nssv3693132, nssv3693144, nssv3693133, nssv3693140, nssv3693156, nssv3693159, nssv3693138, nssv3693147, nssv3693154, nssv3693141, nssv3693137, nssv3693134
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1027504
Frequency
Sample Size11257
Observed Gain21
Observed Loss7
Observed Complex0
Frequencyn/a


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