A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1077254



Internal ID19317218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:156010834..156018035hg38UCSC Ensembl
chrX:155240499..155247700hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg387202
hg197202
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3766201
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1077254
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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