A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6954



Internal ID15205229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:71589852..71623669hg38UCSC Ensembl
OuterchrX:70809702..70843519hg19UCSC Ensembl
OuterchrX:70726427..70760244hg18UCSC Ensembl
OuterchrX:70592723..70626540hg17UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg387180
hg197180
hg187180
hg177180
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv884
SamplesNA19240
Known GenesACRC, BCYRN1, CXCR3
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)nsv6954
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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