A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024606



Internal ID19113823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:64462496..64847603hg38UCSC Ensembl
Innerchr9:69474914..69860021hg19UCSC Ensembl
Innerchr9:68764734..69149841hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38385108
hg19385108
hg18385108
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7655n100
Supporting Variantsnssv3696127
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)nsv1024606
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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