A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015405



Internal ID19104622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39378072..39475440hg38UCSC Ensembl
Innerchr8:39235591..39332959hg19UCSC Ensembl
Innerchr8:39354748..39452116hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3897369
hg1997369
hg1897369
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7171n100
Supporting Variantsnssv3685170, nssv3685171, nssv3685187, nssv3685188, nssv3685172, nssv3685168, nssv3685190, nssv3685177, nssv3685189, nssv3685181, nssv3685185, nssv3685173, nssv3685174, nssv3685178, nssv3685179, nssv3685180, nssv3685176, nssv3685186, nssv3685184, nssv3685169, nssv3685175, nssv3685182, nssv3685183
Samples
Known GenesADAM3A, ADAM5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1015405
Frequency
Sample Size11257
Observed Gain0
Observed Loss23
Observed Complex0
Frequencyn/a


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