A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3758088



Internal ID19056369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:3112966..3156620hg38UCSC Ensembl
Innerchr9:3112966..3156620hg19UCSC Ensembl
Innerchr9:3102966..3146620hg18UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg3843655
hg1943655
hg1843655
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1024242
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)nssv3758088
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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