A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1128412



Internal ID19252200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:139963643..139963764hg38UCSC Ensembl
OuterchrX:139045802..139045923hg19UCSC Ensembl
CytobandXq27.1
Allele length
AssemblyAllele length
hg38122
hg19122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4302n106
Supporting Variantsnssv3958756
SamplesKWS1
Known GenesCXorf66
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1128412
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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