A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1110652



Internal ID19259844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:24183253..24197753hg38UCSC Ensembl
OuterchrY:26329400..26343900hg19UCSC Ensembl
CytobandYq11.23
Allele length
AssemblyAllele length
hg3814501
hg1914501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3960307
SamplesKWS1
Known GenesCSPG4P1Y
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1110652
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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