A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9931



Internal ID15193332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:6220487..9897458hg38UCSC Ensembl
OuterchrY:6088528..9735067hg19UCSC Ensembl
OuterchrY:6148528..10345067hg18UCSC Ensembl
OuterchrY:6131889..10328428hg17UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg383676972
hg193646540
hg184196540
hg174196540
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7473
Supporting Variants
SamplesNA18507
Known GenesAMELY, FAM197Y2, FAM197Y5, PRKY, RBMY1A3P, RBMY3AP, TBL1Y, TSPY1, TSPY10, TSPY2, TSPY3, TSPY4, TSPY8, TTTY1, TTTY11, TTTY12, TTTY16, TTTY18, TTTY19, TTTY1B, TTTY2, TTTY20, TTTY21, TTTY21B, TTTY22, TTTY23, TTTY23B, TTTY2B, TTTY7, TTTY7B, TTTY8, TTTY8B
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)nssv9931
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer