A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9791



Internal ID15539849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:20994127..21042651hg38UCSC Ensembl
OuterchrY:23156013..23204537hg19UCSC Ensembl
OuterchrY:21565401..21613925hg18UCSC Ensembl
OuterchrY:21494138..21542662hg17UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg3848525
hg1948525
hg1848525
hg1748525
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7474
Supporting Variants
SamplesNA18507
Known Genes
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)nssv9791
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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