A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3473195



Internal ID18718663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:22818096..22838263hg38UCSC Ensembl
Innerchr1:23144589..23164756hg19UCSC Ensembl
Innerchr1:23017176..23037343hg18UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg3820168
hg1920168
hg1820168
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1012432
Supporting Variants
Samples
Known GenesEPHB2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3473195
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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