A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3469088



Internal ID18716494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16583102..16788205hg38UCSC Ensembl
Innerchr1:16909597..17114700hg19UCSC Ensembl
Innerchr1:16782184..16987287hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38205104
hg19205104
hg18205104
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1010821
Supporting Variants
Samples
Known GenesCROCCP2, ESPNP, LOC729574, MIR3675, MST1L, MST1P2, NBPF1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3469088
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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