A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2623



Internal ID15193804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:159943689..159976269hg38UCSC Ensembl
Outerchr6:160364721..160397301hg19UCSC Ensembl
Outerchr6:160284711..160317291hg18UCSC Ensembl
Outerchr6:160335132..160367712hg17UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg387431
hg197431
hg187431
hg177431
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5564
Supporting Variants
SamplesNA18555
Known GenesIGF2R
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)nssv2623
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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