A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024707



Internal ID19113924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39378072..39461682hg38UCSC Ensembl
Innerchr8:39235591..39319201hg19UCSC Ensembl
Innerchr8:39354748..39438358hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3883611
hg1983611
hg1883611
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7173n100
Supporting Variantsnssv3685160, nssv3685161
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)nsv1024707
Frequency
Sample Size11257
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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