A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1137696



Internal ID19272281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:113109072..113114272hg38UCSC Ensembl
OuterchrX:112352300..112357500hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg385201
hg195201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3990195
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1137696
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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