A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5739



Internal ID15196992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:34244816..34269239hg38UCSC Ensembl
Outerchr19:34735721..34760144hg19UCSC Ensembl
Outerchr19:39427561..39451984hg18UCSC Ensembl
Outerchr19:39427561..39451984hg17UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg387603
hg197603
hg187603
hg177603
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv2468
Supporting Variants
SamplesNA19129
Known GenesKIAA0355
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)nssv5739
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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