A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003807



Internal ID18746338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16909345..16931063hg38UCSC Ensembl
Innerchr1:17235840..17257558hg19UCSC Ensembl
Innerchr1:17108427..17130145hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3821719
hg1921719
hg1821719
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv123n100
Supporting Variantsnssv3466936
Samples
Known GenesCROCC
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1003807
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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