A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7865813



Internal ID13318088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:55868058..55868072hg38UCSC Ensembl
Innerchr15:55868033..55868097hg38UCSC Ensembl
Outerchr15:55868019..55868111hg38UCSC Ensembl
chr15:56160256..56160270hg19UCSC Ensembl
Innerchr15:56160231..56160295hg19UCSC Ensembl
Outerchr15:56160217..56160309hg19UCSC Ensembl
chr15:53947548..53947562hg18UCSC Ensembl
Innerchr15:53947587..53947523hg18UCSC Ensembl
Outerchr15:53947509..53947601hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3850
hg1950
hg1850
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3374198
Supporting Variants
SamplesNA12005
Known GenesNEDD4
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7865813
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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