A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1115297



Internal ID19267544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:139963637..139963770hg38UCSC Ensembl
OuterchrX:139045796..139045929hg19UCSC Ensembl
CytobandXq27.1
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4302n106
Supporting Variantsnssv3975155, nssv3976346
SamplesKWS2, KWS1
Known GenesCXorf66
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1115297
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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