A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3757604



Internal ID19055885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:61520009..61597238hg38UCSC Ensembl
Innerchr9:44727847..44805076hg19UCSC Ensembl
Innerchr9:44667843..44745072hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3877230
hg1977230
hg1877230
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1023666
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)nssv3757604
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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