A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9682



Internal ID15193435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:16569250..16869192hg38UCSC Ensembl
Outerchr1:16895745..17195687hg19UCSC Ensembl
Outerchr1:16768332..17068274hg18UCSC Ensembl
Outerchr1:16641051..16940993hg17UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38299943
hg19299943
hg18299943
hg17299943
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7173
Supporting Variants
SamplesNA18507
Known GenesCROCCP2, ESPNP, LOC729574, MIR3675, MST1L, 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)nssv9682
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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