A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051625



Internal ID18794156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:112431790..112627148hg38UCSC Ensembl
Innerchr9:115194070..115389428hg19UCSC Ensembl
Innerchr9:114233891..114429249hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38195359
hg19195359
hg18195359
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3695054
Samples
Known GenesHSDL2, KIAA1958
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051625
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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