A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8395



Internal ID15535469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:86959583..86993404hg38UCSC Ensembl
Outerchr7:86588899..86622720hg19UCSC Ensembl
Outerchr7:86426835..86460656hg18UCSC Ensembl
Outerchr7:86233550..86267371hg17UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg385587
hg195587
hg185587
hg175587
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5825
Supporting Variants
SamplesNA12156
Known GenesKIAA1324L
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)nssv8395
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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