A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020625



Internal ID18763160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:37865815..38187846hg38UCSC Ensembl
Innerchr6:37833591..38155622hg19UCSC Ensembl
Innerchr6:37941569..38263600hg18UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg38322032
hg19322032
hg18322032
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3745476
Samples
Known GenesBTBD9, ZFAND3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1020625
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer