A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156507



Internal ID22086908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:61527062..61831160hg38UCSC Ensembl
Outerchr6:61524632..61840446hg38UCSC Ensembl
Innerchr6:62236967..62541065hg19UCSC Ensembl
Outerchr6:62234537..62550351hg19UCSC Ensembl
Cytoband6q11.1
Allele length
AssemblyAllele length
hg38315815
hg19315815
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4018601, nssv4018600
Samples
Known GenesKHDRBS2, MTRNR2L9
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156507
Frequency
Sample Size131
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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