A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998926



Internal ID18811776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:233572564..233611780hg38UCSC Ensembl
Innerchr1:233708310..233747526hg19UCSC Ensembl
Innerchr1:231774933..231814149hg18UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg3839217
hg1939217
hg1839217
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv584n100
Supporting Variantsnssv3502150, nssv3499636, nssv3487875
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)nsv998926
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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