A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6958



Internal ID15551919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:73591007..73619519hg38UCSC Ensembl
OuterchrX:72810843..72839354hg19UCSC Ensembl
OuterchrX:72727568..72756079hg18UCSC Ensembl
OuterchrX:72593864..72622375hg17UCSC Ensembl
CytobandXq13.2
Allele length
AssemblyAllele length
hg3828513
hg1928512
hg1828512
hg1728512
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv9780, nssv886
SamplesNA18507, NA19240
Known GenesCHIC1
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)nsv6958
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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