A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1155920



Internal ID15853582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:146528356..146557568hg38UCSC Ensembl
Innerchr7:146225448..146254660hg19UCSC Ensembl
Innerchr7:145856381..145885593hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3829213
hg1929213
hg1829213
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv608935
Supporting Variants
Samples1780854296_A
Known GenesCNTNAP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1155920
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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