A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3657537



Internal ID18609132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:57788604..58448438hg38UCSC Ensembl
Innerchr6:58082084..58774716hg19UCSC Ensembl
Innerchr6:58190043..58882675hg18UCSC Ensembl
Cytoband6p11.1
Allele length
AssemblyAllele length
hg38659835
hg19692633
hg18692633
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1024377
Supporting Variants
Samples
Known GenesGUSBP4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3657537
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