A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10117



Internal ID15542680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:30579336..30626259hg38UCSC Ensembl
Outerchr17:28906354..28953277hg19UCSC Ensembl
Outerchr17:25930480..25977403hg18UCSC Ensembl
Outerchr17:25930480..25977403hg17UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3846924
hg1946924
hg1846924
hg1746924
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7292
Supporting Variants
SamplesNA18956
Known GenesLRRC37BP1, SH3GL1P2
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)nssv10117
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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