A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1777



Internal ID15194374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:16559350..16715785hg38UCSC Ensembl
Outerchr1:16885845..17042280hg19UCSC Ensembl
Outerchr1:16758432..16914867hg18UCSC Ensembl
Outerchr1:16631151..16787586hg17UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38156436
hg19156436
hg18156436
hg17156436
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7173
Supporting Variants
SamplesNA18555
Known GenesCROCCP2, ESPNP, LOC729574, MIR3675, MST1P2, NBPF1
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)nssv1777
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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