A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021051



Internal ID19110269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:64462496..64886202hg38UCSC Ensembl
Innerchr9:69474914..69898620hg19UCSC Ensembl
Innerchr9:68764734..69188440hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38423707
hg19423707
hg18423707
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7656n100
Supporting Variantsnssv3759738, nssv3696130, nssv3696131
Samples
Known GenesLOC100133920
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1021051
Frequency
Sample Size11257
Observed Gain1
Observed Loss2
Observed Complex0
Frequencyn/a


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