A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7034



Internal ID15205317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:109673490..109713065hg38UCSC Ensembl
OuterchrX:108916719..108956294hg19UCSC Ensembl
OuterchrX:108803375..108842950hg18UCSC Ensembl
OuterchrX:108722864..108762439hg17UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg3839576
hg1939576
hg1839576
hg1739576
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4621
SamplesNA19129
Known GenesACSL4
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)nsv7034
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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