A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998935



Internal ID18811785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109684336..109703496hg38UCSC Ensembl
Innerchr1:110226958..110246118hg19UCSC Ensembl
Innerchr1:110028481..110047641hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3819161
hg1919161
hg1819161
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv269n100
Supporting Variantsnssv3501513, nssv3701945, nssv3701947, nssv3483411, nssv3493749, nssv3498946, nssv3486503, nssv3701946, nssv3498961, nssv3701944, nssv3500507, nssv3494092, nssv3494689, nssv3484949, nssv3494209, nssv3497833, nssv3483692, nssv3490544, nssv3489896, nssv3501627, nssv3490560, nssv3483791, nssv3492340, nssv3490054, nssv3489413, nssv3489936
Samples
Known GenesGSTM1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv998935
Frequency
Sample Size29084
Observed Gain10
Observed Loss16
Observed Complex0
Frequencyn/a


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