A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv957826



Internal ID17306699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:44552494..44552616hg38UCSC Ensembl
OuterchrX:44411740..44411862hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg38123
hg19123
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3002492
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv957826
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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