A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029974



Internal ID19119193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:3107487..3146891hg38UCSC Ensembl
Innerchr9:3107487..3146891hg19UCSC Ensembl
Innerchr9:3097487..3136891hg18UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg3839405
hg1939405
hg1839405
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7377n100
Supporting Variantsnssv3692368, nssv3692369
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)nsv1029974
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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