A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3476834



Internal ID18720548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16691023..16898718hg38UCSC Ensembl
Innerchr1:17017518..17225213hg19UCSC Ensembl
Innerchr1:16890105..17097800hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38207696
hg19207696
hg18207696
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1013663
Supporting Variants
Samples
Known GenesESPNP, LOC729574, MIR3675, MST1L
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3476834
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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