A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10565



Internal ID15195547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:92454423..92486993hg38UCSC Ensembl
Outerchr7:92083737..92116307hg19UCSC Ensembl
Outerchr7:91921673..91954243hg18UCSC Ensembl
Outerchr7:91728388..91760958hg17UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg386938
hg196938
hg186938
hg176938
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5840
Supporting Variants
SamplesNA18956
Known GenesGATAD1
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nssv10565
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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