A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7157



Internal ID15552138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:152404075..152436166hg38UCSC Ensembl
OuterchrX:151572547..151604638hg19UCSC Ensembl
OuterchrX:151323203..151355294hg18UCSC Ensembl
OuterchrX:151243115..151275206hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg387344
hg197344
hg187344
hg177344
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6389
SamplesNA12156
Known GenesGABRA3
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)nsv7157
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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