A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998503



Internal ID18811353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:25269902..25335502hg38UCSC Ensembl
Innerchr1:25596393..25661993hg19UCSC Ensembl
Innerchr1:25468980..25534580hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3865601
hg1965601
hg1865601
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv141n100
Supporting Variantsnssv3477529, nssv3475147, nssv3470169, nssv3481480, nssv3468384, nssv3475110, nssv3468903, nssv3464382, nssv3465043, nssv3464744, nssv3475853, nssv3700489, nssv3469531, nssv3466206, nssv3463141, nssv3475326, nssv3463683, nssv3700491, nssv3700490, nssv3471230, nssv3475777, nssv3481351, nssv3466612, nssv3471079, nssv3700488
Samples
Known GenesRHD
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv998503
Frequency
Sample Size29084
Observed Gain0
Observed Loss25
Observed Complex0
Frequencyn/a


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