A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5840



Internal ID15204004
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 StatusM
Merged Variants
Supporting Variantsnssv10565
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)nsv5840
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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