A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034224



Internal ID19123446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:39445501..39878557hg38UCSC Ensembl
Innerchr9:41475094..42023575hg19UCSC Ensembl
Innerchr9:41465094..42013575hg18UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg38433057
hg19548482
hg18548482
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7542n100
Supporting Variantsnssv3690175, nssv3690186, nssv3690190, nssv3690192, nssv3690180, nssv3690181, nssv3690188, nssv3690185, nssv3690179, nssv3690193, nssv3690173, nssv3690178, nssv3690182, nssv3690187, nssv3690174, nssv3690184, nssv3690176, nssv3690189, nssv3690183, nssv3690172, nssv3690177, nssv3690191
Samples
Known GenesKGFLP2, LOC643648, LOC653501, MGC21881, SPATA31A5, SPATA31A7, ZNF658B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1034224
Frequency
Sample Size11257
Observed Gain22
Observed Loss0
Observed Complex0
Frequencyn/a


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