A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031956



Internal ID19121178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39426730..39505415hg38UCSC Ensembl
Innerchr8:39284249..39362934hg19UCSC Ensembl
Innerchr8:39403406..39482091hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3878686
hg1978686
hg1878686
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7178n100
Supporting Variantsnssv3685949, nssv3685948
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)nsv1031956
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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