A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022153



Internal ID19111371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:154997968..155041357hg38UCSC Ensembl
Innerchr7:154789678..154833067hg19UCSC Ensembl
Innerchr7:154420611..154464000hg18UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg3843390
hg1943390
hg1843390
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3674664
Samples
Known GenesPAXIP1, PAXIP1-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1022153
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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