A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1128534



Internal ID18936205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:44531247..44531335hg38UCSC Ensembl
OuterchrX:44390493..44390581hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3960433
SamplesKWS1
Known GenesFUNDC1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1128534
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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