A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3975652



Internal ID18858691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:1560478..1560555hg38UCSC Ensembl
Outerchr10:1602673..1602750hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1124351
Supporting Variants
SamplesKWS1
Known GenesADARB2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3975652
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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