A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019950



Internal ID19109168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39445895..39527663hg38UCSC Ensembl
Innerchr8:39303414..39385182hg19UCSC Ensembl
Innerchr8:39422571..39504339hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3881769
hg1981769
hg1881769
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7181n100
Supporting Variantsnssv3687204
Samples
Known GenesADAM3A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019950
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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