A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001379



Internal ID18743910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16883096..16931632hg38UCSC Ensembl
Innerchr1:17209591..17258127hg19UCSC Ensembl
Innerchr1:17082178..17130714hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3848537
hg1948537
hg1848537
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv115n100
Supporting Variantsnssv3466810
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)nsv1001379
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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