A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038600



Internal ID18781131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:69482727..69503518hg38UCSC Ensembl
Innerchr9:72097643..72118434hg19UCSC Ensembl
Innerchr9:71287463..71308254hg18UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3820792
hg1920792
hg1820792
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7672n100
Supporting Variantsnssv3696260, nssv3696255, nssv3696264, nssv3696254, nssv3696263, nssv3696253, nssv3696257, nssv3696261, nssv3696262, nssv3696258, nssv3696256, nssv3759752, nssv3696259
Samples
Known GenesAPBA1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038600
Frequency
Sample Size29084
Observed Gain4
Observed Loss9
Observed Complex0
Frequencyn/a


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