A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3692368



Internal ID18990649
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 StatusS
Merged Variantsnsv1029974
Supporting Variants
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)nssv3692368
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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