A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3468311



Internal ID18716084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16888315..16931063hg38UCSC Ensembl
Innerchr1:17214810..17257558hg19UCSC Ensembl
Innerchr1:17087397..17130145hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3842749
hg1942749
hg1842749
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1002932
Supporting Variants
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)nssv3468311
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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