A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046704



Internal ID19135923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34435409..34563605hg38UCSC Ensembl
Innerchr15:34727610..34855806hg19UCSC Ensembl
Innerchr15:32514902..32643098hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38128197
hg19128197
hg18128197
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2563n100
Supporting Variantsnssv3551537, nssv3551533, nssv3551526, nssv3551530, nssv3551539, nssv3551524, nssv3551523, nssv3551540, nssv3551522, nssv3716615, nssv3551527, nssv3716618, nssv3716613, nssv3551543, nssv3551541, nssv3551538, nssv3551520, nssv3551525, nssv3551535, nssv3551531, nssv3716617, nssv3551544, nssv3716614, nssv3716612, nssv3551521, nssv3551532, nssv3551529, nssv3551528, nssv3551542, nssv3716616, nssv3551536, nssv3551534
Samples
Known GenesGOLGA8A, GOLGA8B, MIR1233-1, MIR1233-2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046704
Frequency
Sample Size11257
Observed Gain0
Observed Loss32
Observed Complex0
Frequencyn/a


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