A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1000171



Internal ID18742702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16930810..16965387hg38UCSC Ensembl
Innerchr1:17257305..17291882hg19UCSC Ensembl
Innerchr1:17129892..17164469hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3834578
hg1934578
hg1834578
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv127n100
Supporting Variantsnssv3464099
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)nsv1000171
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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