A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3765596



Internal ID18967922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:135973540..135976741hg38UCSC Ensembl
chrX:135055699..135058900hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg383202
hg193202
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1076276
Supporting Variants
SamplesKWP1
Known GenesMMGT1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3765596
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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