A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3870



Internal ID15191911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:16618646..16638076hg38UCSC Ensembl
Outerchr1:16945141..16964571hg19UCSC Ensembl
Outerchr1:16817728..16837158hg18UCSC Ensembl
Outerchr1:16690447..16709877hg17UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg385580
hg195580
hg185580
hg175580
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3854
Supporting Variants
SamplesNA12878
Known GenesCROCCP2
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)nssv3870
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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