A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9837



Internal ID15193218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:52302336..52331241hg38UCSC Ensembl
Outerchr12:52696120..52725025hg19UCSC Ensembl
Outerchr12:50982387..51011292hg18UCSC Ensembl
Outerchr12:50982387..51011292hg17UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg3828906
hg1928906
hg1828906
hg1728906
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7230
Supporting Variants
SamplesNA18507
Known GenesKRT83, KRT86
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)nssv9837
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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