A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027972



Internal ID19117190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:42727697..42856259hg38UCSC Ensembl
Innerchr9:44114860..44243422hg19UCSC Ensembl
Innerchr9:44054856..44183418hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38128563
hg19128563
hg18128563
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7573n100
Supporting Variantsnssv3693004, nssv3756852
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)nsv1027972
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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