A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6961



Internal ID15551923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:75659306..75704021hg38UCSC Ensembl
OuterchrX:74879141..74923856hg19UCSC Ensembl
OuterchrX:74795866..74840581hg18UCSC Ensembl
OuterchrX:74662162..74706877hg17UCSC Ensembl
CytobandXq13.3
Allele length
AssemblyAllele length
hg3844716
hg1944716
hg1844716
hg1744716
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8742
SamplesNA12156
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)nsv6961
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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