A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3699577



Internal ID18997858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:72542484..72622475hg38UCSC Ensembl
Innerchr1:73008167..73088158hg19UCSC Ensembl
Innerchr1:72780755..72860746hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3879992
hg1979992
hg1879992
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1000359
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3699577
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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