A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034997



Internal ID19124216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:7731398..7773114hg38UCSC Ensembl
Innerchr9:7731398..7773114hg19UCSC Ensembl
Innerchr9:7721398..7763114hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3841717
hg1941717
hg1841717
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7393n100
Supporting Variantsnssv3689111, nssv3689110
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)nsv1034997
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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