A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004321



Internal ID19093538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:35762271..35900266hg38UCSC Ensembl
Innerchr3:35803763..35941758hg19UCSC Ensembl
Innerchr3:35778767..35916762hg18UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38137996
hg19137996
hg18137996
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4717n100
Supporting Variantsnssv3589611, nssv3739682, nssv3739677, nssv3739679, nssv3739686, nssv3589622, nssv3589613, nssv3589623, nssv3739681, nssv3589625, nssv3589624, nssv3739684, nssv3589632, nssv3589610, nssv3589616, nssv3589627, nssv3589617, nssv3589614, nssv3589620, nssv3589621, nssv3589618, nssv3589629, nssv3589619, nssv3739683, nssv3739678, nssv3589615, nssv3589626, nssv3739685, nssv3589631, nssv3739680, nssv3589628, nssv3589612, nssv3589630
Samples
Known GenesARPP21
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1004321
Frequency
Sample Size11257
Observed Gain33
Observed Loss0
Observed Complex0
Frequencyn/a


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