A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3804



Internal ID15538531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:81839285..81861869hg38UCSC Ensembl
OuterchrX:81094784..81117368hg19UCSC Ensembl
OuterchrX:80981440..81004024hg18UCSC Ensembl
OuterchrX:80900929..80923513hg17UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg3822585
hg1922585
hg1822585
hg1722585
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv6975
Supporting Variants
SamplesNA12878
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)nssv3804
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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