A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026865



Internal ID19116083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39378072..39540213hg38UCSC Ensembl
Innerchr8:39235591..39397732hg19UCSC Ensembl
Innerchr8:39354748..39516889hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38162142
hg19162142
hg18162142
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7170n100
Supporting Variantsnssv3687592, nssv3687596, nssv3687589, nssv3687590, nssv3687597, nssv3687594, nssv3687599, nssv3687588, nssv3687586, nssv3687593, nssv3687598, nssv3687595, nssv3687585, nssv3687591, nssv3687600, nssv3687587
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)nsv1026865
Frequency
Sample Size11257
Observed Gain13
Observed Loss3
Observed Complex0
Frequencyn/a


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