A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170261



Internal ID21314322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:7346359..7476823hg38UCSC Ensembl
Outerchr1:7342442..7477440hg38UCSC Ensembl
Innerchr1:7406419..7536883hg19UCSC Ensembl
Outerchr1:7402502..7537500hg19UCSC Ensembl
Innerchr1:7329006..7459470hg18UCSC Ensembl
Outerchr1:7325089..7460087hg18UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg38134999
hg19134999
hg18134999
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14241679, nssv14244500
SamplesNGO_25, NGO_23
Known GenesCAMTA1
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170261
Frequency
Sample Size93
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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