A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3700333



Internal ID18651928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:25269444..25351874hg38UCSC Ensembl
Innerchr1:25595935..25678365hg19UCSC Ensembl
Innerchr1:25468522..25550952hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3882431
hg1982431
hg1882431
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv999016
Supporting Variants
Samples
Known GenesRHD, TMEM50A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3700333
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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