A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021938



Internal ID19111156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:64683555..64965592hg38UCSC Ensembl
Innerchr9:69695973..69978010hg19UCSC Ensembl
Innerchr9:68985793..69267830hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38282038
hg19282038
hg18282038
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3696166, nssv3696171, nssv3696172, nssv3696169, nssv3696167, nssv3696170, nssv3696168
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)nsv1021938
Frequency
Sample Size11257
Observed Gain1
Observed Loss6
Observed Complex0
Frequencyn/a


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